Literature DB >> 35165296

Whole genome sequences of 234 indigenous African chickens from Ethiopia.

Almas Gheyas1, Adriana Vallejo-Trujillo2, Adebabay Kebede3,4, Tadelle Dessie3, Olivier Hanotte2,3, Jacqueline Smith5.   

Abstract

Indigenous chickens predominate poultry production in Africa. Although preferred for backyard farming because of their adaptability to harsh tropical environments, these populations suffer from relatively low productivity compared to commercial lines. Genome analyses can unravel the genetic potential of improvement of these birds for both production and resilience traits for the benefit of African poultry farming systems. Here we report whole-genome sequences of 234 indigenous chickens from 24 Ethiopian populations distributed under diverse agro-climatic conditions. The data represents over eight terabytes of paired-end sequences from the Ilumina HiSeqX platform with an average coverage of about 57X. Almost 99% of the sequence reads could be mapped against the chicken reference genome (GRCg6a), confirming the high quality of the data. Variant calling detected around 15 million SNPs, of which about 86% are known variants (i.e., present in public databases), providing further confidence on the data quality. The dataset provides an excellent resource for investigating genetic diversity and local environmental adaptations with important implications for breed improvement and conservation purposes.
© 2022. Crown.

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Year:  2022        PMID: 35165296      PMCID: PMC8844291          DOI: 10.1038/s41597-022-01129-4

Source DB:  PubMed          Journal:  Sci Data        ISSN: 2052-4463            Impact factor:   6.444


Background & Summary

Poultry farming constitutes an important economic activity across Africa, providing a livelihood for millions of people. However, the lion’s share of the poultry production in most countries still comes from smallholder backyard indigenous poultry reared under scavenging or semi-scavenging conditions, with no or limited human intervention (e.g., secured sheltering at night, supplementary feeding, or vaccination)[1,2]. Ethiopia is one of the sub-Saharan African countries where chicken farming plays a crucial role in the country’s sociocultural context and economy, with ~97% of the production still coming from “extensive” farming practice of local birds. Domestic chickens were originally introduced into Ethiopia from Asia from around 3000 years ago[3,4]. Since their introduction, chicken populations have been dispersed throughout the country and, over time, have adapted to thrive in its diverse agro-ecologies. These birds, now considered as indigenous, show greater resistance to various local poultry diseases and parasites compared to exotic and commercially improved chickens. Due to their superior adaptability to local tropical environmental conditions as well as their foraging ability and broodiness, these indigenous birds are often preferred by smallholder farmers for backyard rearing[2,5,6]. However, in the absence of proper management practices or any systematic selection efforts, local birds generally show poorer productivity but higher survivability compared to the commercial counterparts. Their untapped genetic potential can be utilized for improving their performance. Genome analyses can unravel the genetic diversity of indigenous chicken populations and provide the basis for genetic improvements for better production and performance. Moreover, genome analysis of populations from different agro-ecological zones can elucidate the genetic basis of local environmental adaptation. Resilient genotypes, identified from such studies, can then be selected for or introgressed in improved productive breeds for superior performance under local climate. The Ethiopian landscape can be considered a microcosm of different agro-ecologies encountered in Africa due to extreme variations in its altitudinal topography and rainfall pattern. This has given rise to diverse agro-climate zones in the country, ranging from hot-arid and hot-humid to cold-humid and cold-arid[7]. Therefore, genomic analysis of Ethiopian chicken populations is particularly pertinent for elucidating their local adaptation. This article reports whole genome sequencing data from hundreds of indigenous chickens (n = 234), sampled from 24 different Ethiopian villages or populations distributed under diverse agro-ecological and climatic conditions [Table 1; also see Fig. 1A,B and supplementary Table S1 in the study by Gheyas et al.[8]]. The study also reports about 15 million Single Nucleotide Polymorphisms (SNPs) detected by mapping the sequencing data against the chicken reference genome (GRCg6a; https://www.ncbi.nlm.nih.gov/assembly/?term=GCA_000002315.5). Sequencing has been performed at a very high coverage (average 57X), increasing the power and resolution of genomic analyses. Although most of the reported variants are already known (only 14% are novel), the associated VCF file (submitted to European Variant Archive) shows genotype data for individual samples; therefore it offers an excellent resource for a variety of population genetics analyses. Some of these sequences and variant data have been used in a recent study to elucidate the genome-environmental adaptation in Ethiopian chickens[8].
Table 1

Details of Ethiopian chicken populations.

Population IDs as appear in ENA databaseNo. of samplesGeographic regionDistrictVillage or Kebele
Afar;Dulecha;Hugub10AfarDulechaHugub
Afar;Dulecha;Kefis10AfarDulechaKefis
Amhara;Banja;Surta9AmharaBanjaSurta
Amhara;FagitaLekoma;AmeshaShinkuri10AmharaFagita LekomaAmesha Shinkuri
Amhara;FagitaLekoma;Batambie8AmharaFagita LekomaBatambie
Amhara;FagitaLekoma;Gafera10AmharaFagita LekomaGafera
Amhara;GondarZuria;TsionTeguaz10AmharaGondar ZuriaTsionTeguaz
Amhara;Kalu;0–25Adane10AmharaKalu0–25Adane
Amhara;Kalu;Arabo10AmharaKaluArabo
Amhara;MenzGeraMidir;AlfaMidir/05/10AmharaMenz Gera MidirAlfa Midir/05/
Amhara;MenzGeraMidir;NegasiAmba/07/10AmharaMenz Gera MidirNegasi Amba/07/
Amhara;SouthAchefer;Ashuda10AmharaSouth AcheferAshuda
Amhara;SouthAchefer;Dikuli10AmharaSouth AcheferDikuli
Gumuz;Dibate;Gesses10GumuzDibateGesses
Gumuz;Dibate;Kido9GumuzDibateKido
Oromia;Dugda;BekeleGirissa10OromiaDugdaBekele Girissa
Oromia;Dugda;ShubiGemo10OromiaDugdaShubi Gemo
SNNPR;Dara;Kumato10SNNPRDaraKumato
SNNPR;Dara;Loya10SNNPRDaraLoya
Tigray;Enderta;Meseret10TigrayEndertaMeseret
Tigray;Merebleke;HadushAdi9TigrayMereblekeHadush Adi
Tigray;Merebleke;Mihquan10TigrayMereblekeMihquan
Tigray;SaharetiSamire;Gijet9TigraySahareti SamireGijet
Tigray;SaharetiSamire;Metkilimat10TigraySahareti SamireMetkilimat

$Also see Supplementary Table S1 in Gheyas et al.[8].

Fig. 1

Overview of the sequence mapping, variant calling and variant filtration pipeline. The pipeline follows GATK best practice protocol for germline short variant discovery[18].

Details of Ethiopian chicken populations. $Also see Supplementary Table S1 in Gheyas et al.[8]. Overview of the sequence mapping, variant calling and variant filtration pipeline. The pipeline follows GATK best practice protocol for germline short variant discovery[18]. The data are expected to have many utilities, ranging from exploring genetic diversity, identifying signatures of positive selection, analysing genome-environment associations, finding genetic variants from regions of interests (e.g., within or near candidate genes or QTLs associated with disease and production traits), exploring different types of genetic variants (e.g., small insertions/deletions, structural variants, avian retroviral elements), and for developing tools for genomic analysis (e.g., high or low density SNP genotyping arrays for use in breeding programmes). Furthermore, the data represent the largest number of indigenous chicken samples sequenced from an African country. Only a few studies have previously reported such large scale sequencing of chicken samples but none generated such large scale African data[9-12]. These data are therefore a rich addition to global chicken genome sequence databases and can be used in conjunction with sequencing data from other countries/regions around the globe for studying demographic and domestication histories in chicken.

Methods

Chicken sampling

Chicken sampling considered different agro-climatic conditions and geographic regions of Ethiopia. Sampling of local foraging chickens was performed from 24 villages or ‘kebeles’ from across six regional states – Afar, Amhara, Gumuz, Oromia, SNNPR (Southern Nations, Nationalities and Peoples’ Region), and Tigray, representing diverse agro-climatic and ecological conditions observed in Ethiopia. Each village was considered as a separate population. To capture genetic diversity within populations, 8 to 10 chicken samples were collected from each village (Table 1). Sampling was performed by drawing blood (50–250 µl) from the wing vein of each bird with syringes using cryotubes filled with 1.5 ml absolute ethanol (100%) following the guidelines available at https://www.sheffield.ac.uk/nbaf-s/protocols_list. The samples consisted of 146 female and 88 male birds (total 234) and varied in their age (4–30 months; average 10.3 months) and body weight (0.6–2.6 kg, average 1.27 kg). The samples were collected with the logistical support and agreement of the Ethiopian Ministry of Agriculture and Ethiopian Institute of Agricultural Research (EIAR). All animal works were approved by the Institutional Animal Care and Use Committee of the International Livestock Research Institute (IREC2017-26). The sample information has been submitted to the European Nucleotide Archive (ENA) under the study accession PRJEB39275[13] (see Online-only Table 1 for details about the samples).
Online-only Table 1

Ethiopian indigenous chicken samples analysed.

Sample IDENA study accessionENA sample accessionGeographic regionDistrictVillage or kebeleRead pairs sequencedYield (Gb)Yield Q30 (Gb)Average coverage (X)SexEstimated age (month)body weight (kg)
ABB-2H_PinkPRJEB39275SAMEA7050617AmharaFagita LekomaBatambie236903685715767F121.5
ABB-3CPRJEB39275SAMEA7050618AmharaFagita LekomaBatambie136048918413238M81.75
ABB-4H1PRJEB39275SAMEA7050619AmharaFagita LekomaBatambie241166137725868F71
ABB-4H2PRJEB39275SAMEA7050620AmharaFagita LekomaBatambie3464596371038498F71
ABB-5H1PRJEB39275SAMEA7050621AmharaFagita LekomaBatambie233217499705666F121.8
ABB-6Cock1PRJEB39275SAMEA7050622AmharaFagita LekomaBatambie273287822826777M61
ABB-6H2PRJEB39275SAMEA7050623AmharaFagita LekomaBatambie235530885705866F121.8
ABB-6H3PRJEB39275SAMEA7050624AmharaFagita LekomaBatambie152188006453643F101
ABS-1CPRJEB39275SAMEA7050625AmharaBanjaSurta245482239735969M81.5
ABS-1HPRJEB39275SAMEA7050626AmharaBanjaSurta216663455655261F101.5
ABS-2HPRJEB39275SAMEA7050627AmharaBanjaSurta231834678695565F71.5
ABS-3CPRJEB39275SAMEA7050628AmharaBanjaSurta254625156766072M51.5
ABS-4CPRJEB39275SAMEA7050629AmharaBanjaSurta239438827725767M61.8
ABS-5H1PRJEB39275SAMEA7050630AmharaBanjaSurta198637437594756F121
ABS-5H2PRJEB39275SAMEA7050631AmharaBanjaSurta270614377816576F141.5
ABS-6HPRJEB39275SAMEA7050632AmharaBanjaSurta224653163655163F92
ABS-7HPRJEB39275SAMEA7050633AmharaBanjaSurta231822222695665F82
AFA-1CPRJEB39275SAMEA7050634AmharaFagita LekomaAmesha Shinkuri159125452483745M121
AFA-1HPRJEB39275SAMEA7050635AmharaFagita LekomaAmesha Shinkuri202087813604957F131.5
AFA-2HPRJEB39275SAMEA7050636AmharaFagita LekomaAmesha Shinkuri237574115715767F121.5
AFA-3CPRJEB39275SAMEA7050637AmharaFagita LekomaAmesha Shinkuri246350017746069M51
AFA-4CPRJEB39275SAMEA7050638AmharaFagita LekomaAmesha Shinkuri239431575725767M61.5
AFA-4HPRJEB39275SAMEA7050639AmharaFagita LekomaAmesha Shinkuri170867009514048F121.5
AFA-5CPRJEB39275SAMEA7050640AmharaFagita LekomaAmesha Shinkuri235330808705666M71.5
AFA-6HPRJEB39275SAMEA7050641AmharaFagita LekomaAmesha Shinkuri238841700715867F121
AFA-7HPRJEB39275SAMEA7050642AmharaFagita LekomaAmesha Shinkuri248000703746170F81
AFA-8HPRJEB39275SAMEA7050643AmharaFagita LekomaAmesha Shinkuri147424380443542F71
AFDH-C1PRJEB39275SAMEA7050644AfarDulechaHugub202434489614757M241.4
AFDH-C3PRJEB39275SAMEA7050645AfarDulechaHugub156927338473744M1
AFDH-C5PRJEB39275SAMEA7050646AfarDulechaHugub155819772473744F80.9
AFDH-C7PRJEB39275SAMEA7050647AfarDulechaHugub194400157584655M
AFDH-H1PRJEB39275SAMEA7050648AfarDulechaHugub191026735574454M
AFDH-H2PRJEB39275SAMEA7050649AfarDulechaHugub151570048453543F121.6
AFDH-H4PRJEB39275SAMEA7050650AfarDulechaHugub217737906644961F
AFDH-H6PRJEB39275SAMEA7050651AfarDulechaHugub174428592524149F50.8
AFDH-H8PRJEB39275SAMEA7050652AfarDulechaHugub170865081514048F70.9
AFDH-H9PRJEB39275SAMEA7050653AfarDulechaHugub176562813534450F241.3
AFDK-C1PRJEB39275SAMEA7050654AfarDulechaKefis196898525574555M
AFDK-C2PRJEB39275SAMEA7050655AfarDulechaKefis481693349144113136M1.4
AFDK-C3PRJEB39275SAMEA7050656AfarDulechaKefis444457131133101125M1.05
AFDK-H10PRJEB39275SAMEA7050657AfarDulechaKefis173434225524249F120.97
AFDK-H4PRJEB39275SAMEA7050658AfarDulechaKefis160968698483845F71.7
AFDK-H5PRJEB39275SAMEA7050659AfarDulechaKefis167502638503847F71
AFDK-H6PRJEB39275SAMEA7050660AfarDulechaKefis195647263584555F80.6
AFDK-H7PRJEB39275SAMEA7050661AfarDulechaKefis151191455453643F81
AFDK-H8PRJEB39275SAMEA7050662AfarDulechaKefis165552066494047F121.4
AFDK-H9PRJEB39275SAMEA7050663AfarDulechaKefis155092561463544F1.2
AFG-1HPRJEB39275SAMEA7050664AmharaFagita LekomaGafera256197086776372F61.5
AFG-2C1PRJEB39275SAMEA7050665AmharaFagita LekomaGafera283120181856880M61.5
AFG-2HPRJEB39275SAMEA7050666AmharaFagita LekomaGafera265669387796575F61.5
AFG-3CPRJEB39275SAMEA7050667AmharaFagita LekomaGafera270092780816576M51.5
AFG-3HPRJEB39275SAMEA7050668AmharaFagita LekomaGafera143021468433440F81.5
AFG-4H_P_YPRJEB39275SAMEA7050669AmharaFagita LekomaGafera171882362514248F71.5
AFG-5CPRJEB39275SAMEA7050670AmharaFagita LekomaGafera236189159715867M61.5
AFG-5HPRJEB39275SAMEA7050671AmharaFagita LekomaGafera280842991846879F41
AFG-6HPRJEB39275SAMEA7050672AmharaFagita LekomaGafera194232239584755F41
AFG-8CPRJEB39275SAMEA7050673AmharaFagita LekomaGafera276246879836778M51
AGT-10CPRJEB39275SAMEA7050674AmharaGondar ZuriaTsion Teguaz174781192524149M81
AGT-1CPRJEB39275SAMEA7050675AmharaGondar ZuriaTsion Teguaz162035613483846M191.5
AGT-2CPRJEB39275SAMEA7050676AmharaGondar ZuriaTsion Teguaz166589303503947M81.5
AGT-3HPRJEB39275SAMEA7050677AmharaGondar ZuriaTsion Teguaz178769791534350F121.5
AGT-4HPRJEB39275SAMEA7050678AmharaGondar ZuriaTsion Teguaz240100167725868F121
AGT-5HPRJEB39275SAMEA7050679AmharaGondar ZuriaTsion Teguaz164846479493946F121
AGT-6HPRJEB39275SAMEA7050680AmharaGondar ZuriaTsion Teguaz171572055514148F151
AGT-7HPRJEB39275SAMEA7050681AmharaGondar ZuriaTsion Teguaz158099542473745F181
AGT-8HPRJEB39275SAMEA7050682AmharaGondar ZuriaTsion Teguaz160926681483845F91
AGT-9CPRJEB39275SAMEA7050683AmharaGondar ZuriaTsion Teguaz158368711473745M91.5
AK025A-10C-059PRJEB39275SAMEA7050684AmharaKalu0-25Adane221676963665262M61.1
AK025A-1HC-55PRJEB39275SAMEA7050685AmharaKalu0-25Adane214924783645261F121.1
AK025A-2H-149PRJEB39275SAMEA7050686AmharaKalu0-25Adane170277513514148F80.88
AK025A-3H-85PRJEB39275SAMEA7050687AmharaKalu0-25Adane211196221634959F71.4
AK025A-4H-070PRJEB39275SAMEA7050688AmharaKalu0-25Adane171437883514148F1.06
AK025A-5H-71PRJEB39275SAMEA7050689AmharaKalu0-25Adane154447981463743F60.86
AK025A-6H-97PRJEB39275SAMEA7050690AmharaKalu0-25Adane156387764473744F111.14
AK025A-7C1PRJEB39275SAMEA7050691AmharaKalu0-25Adane164065755493846M81.2
AK025A-8CPRJEB39275SAMEA7050692AmharaKalu0-25Adane238209857715667M
AK025A-8C-50PRJEB39275SAMEA7050693AmharaKalu0-25Adane171979726514248M81.34
AKA-10H-11PRJEB39275SAMEA7050694AmharaKaluArabo156126238473544F1.1
AKA-1CPRJEB39275SAMEA7050695AmharaKaluArabo161880229483846M0.9
AKA-2HPRJEB39275SAMEA7050696AmharaKaluArabo146145065443441F50.82
AKA-3CPRJEB39275SAMEA7050697AmharaKaluArabo43708024613199123M51.14
AKA-4HPRJEB39275SAMEA7050698AmharaKaluArabo164770789494046F121.2
AKA-5HPRJEB39275SAMEA7050699AmharaKaluArabo172851099524249F60.85
AKA-6HPRJEB39275SAMEA7050700AmharaKaluArabo181386777544351F81.2
AKA-7CPRJEB39275SAMEA7050701AmharaKaluArabo153111811463643M81.2
AKA-8HPRJEB39275SAMEA7050702AmharaKaluArabo147763907443542F141.3
AKA-9CPRJEB39275SAMEA7050703AmharaKaluArabo153394599463443M81.5
AMAM-10H-108PRJEB39275SAMEA7050704AmharaMenz Gera MidirAlfa Midir/05/219841013665362F71
AMAM-1H-031PRJEB39275SAMEA7050705AmharaMenz Gera MidirAlfa Midir/05/185325710554452F241.12
AMAM-2C-151PRJEB39275SAMEA7050706AmharaMenz Gera MidirAlfa Midir/05/167703397504147M121.01
AMAM-3H-124PRJEB39275SAMEA7050707AmharaMenz Gera MidirAlfa Midir/05/213711633644860F140.7
AMAM-4H-115PRJEB39275SAMEA7050708AmharaMenz Gera MidirAlfa Midir/05/174718288523949F81.26
AMAM-5C-147PRJEB39275SAMEA7050709AmharaMenz Gera MidirAlfa Midir/05/165835363503847M91.38
AMAM-6H-120PRJEB39275SAMEA7050710AmharaMenz Gera MidirAlfa Midir/05/189256702574353F91.08
AMAM-7C-116PRJEB39275SAMEA7050711AmharaMenz Gera MidirAlfa Midir/05/221757177665362M61.16
AMAM-8H-101PRJEB39275SAMEA7050712AmharaMenz Gera MidirAlfa Midir/05/173924627524049F120.78
AMAM-9C-107PRJEB39275SAMEA7050713AmharaMenz Gera MidirAlfa Midir/05/169714035513948M91.52
AMNA-10CPRJEB39275SAMEA7050714AmharaMenz Gera MidirNegasi Amba/07/181657517544451M121.32
AMNA-1H-102PRJEB39275SAMEA7050715AmharaMenz Gera MidirNegasi Amba/07/208716330625059F121.18
AMNA-2C-104PRJEB39275SAMEA7050716AmharaMenz Gera MidirNegasi Amba/07/173300406524049M121.2
AMNA-3H-170PRJEB39275SAMEA7050717AmharaMenz Gera MidirNegasi Amba/07/178208155534050F121.04
AMNA-4H-121PRJEB39275SAMEA7050718AmharaMenz Gera MidirNegasi Amba/07/170292167514048F121.1
AMNA-5C-138PRJEB39275SAMEA7050719AmharaMenz Gera MidirNegasi Amba/07/173866786523949M150.98
AMNA-6H-165PRJEB39275SAMEA7050720AmharaMenz Gera MidirNegasi Amba/07/211546437634960F11.51
AMNA-7H-144PRJEB39275SAMEA7050721AmharaMenz Gera MidirNegasi Amba/07/154462951463743F91.2
AMNA-8HPRJEB39275SAMEA7050722AmharaMenz Gera MidirNegasi Amba/07/203003582614957M
AMNA-9C-171PRJEB39275SAMEA7050723AmharaMenz Gera MidirNegasi Amba/07/172104718514248M121.7
ASA-10HPRJEB39275SAMEA7050724AmharaSouth AcheferAshuda257638319776273F81.5
ASA-1CPRJEB39275SAMEA7050725AmharaSouth AcheferAshuda275105168826877M61.5
ASA-2HPRJEB39275SAMEA7050726AmharaSouth AcheferAshuda171251993514048F81
ASA-3HPRJEB39275SAMEA7050727AmharaSouth AcheferAshuda186056888564552F81
ASA-4CPRJEB39275SAMEA7050728AmharaSouth AcheferAshuda240955666725868M51.5
ASA-5HPRJEB39275SAMEA7050729AmharaSouth AcheferAshuda238719443715967F81
ASA-6HPRJEB39275SAMEA7050730AmharaSouth AcheferAshuda209755600635159F91
ASA-7HPRJEB39275SAMEA7050731AmharaSouth AcheferAshuda157731335473844F111.5
ASA-8CPRJEB39275SAMEA7050732AmharaSouth AcheferAshuda237053984715767M71.5
ASA-9CPRJEB39275SAMEA7050733AmharaSouth AcheferAshuda196938915594855M61.5
ASD-1CPRJEB39275SAMEA7050734AmharaSouth AcheferDikuli160638411483845M91.5
ASD-1HPRJEB39275SAMEA7050735AmharaSouth AcheferDikuli199066825594856F91
ASD-2CPRJEB39275SAMEA7050736AmharaSouth AcheferDikuli219215794655362M182
ASD-2HPRJEB39275SAMEA7050737AmharaSouth AcheferDikuli151513421453543F91
ASD-3HPRJEB39275SAMEA7050738AmharaSouth AcheferDikuli161665189483846F91.5
ASD-4HPRJEB39275SAMEA7050739AmharaSouth AcheferDikuli159930126483745F101
ASD-5CPRJEB39275SAMEA7050740AmharaSouth AcheferDikuli255279427766272M121
ASD-6HPRJEB39275SAMEA7050741AmharaSouth AcheferDikuli285006193856980F121.5
ASD-7HPRJEB39275SAMEA7050742AmharaSouth AcheferDikuli175380650524249F121.5
ASD-8CPRJEB39275SAMEA7050743AmharaSouth AcheferDikuli256119589776372M91.5
BGDG-10HPRJEB39275SAMEA7050744GumuzDibateGesses207820060624959F
BGDG-1C-080PRJEB39275SAMEA7050745GumuzDibateGesses208589648625059M1.48
BGDG-2C-95PRJEB39275SAMEA7050746GumuzDibateGesses167721494504147M0.92
BGDG-3H-12PRJEB39275SAMEA7050747GumuzDibateGesses168341912503947F81
BGDG-4C-51PRJEB39275SAMEA7050748GumuzDibateGesses159377844483745M1.9
BGDG-5H-2PRJEB39275SAMEA7050749GumuzDibateGesses168898025503948F121
BGDG-6CPRJEB39275SAMEA7050750GumuzDibateGesses263030959766174M
BGDG-7H-23PRJEB39275SAMEA7050751GumuzDibateGesses181115763544251F1
BGDG-8HPRJEB39275SAMEA7050752GumuzDibateGesses222615507665363F71.25
BGDG-9HPRJEB39275SAMEA7050753GumuzDibateGesses175232510524249F91.4
BGDK-10C-14PRJEB39275SAMEA7050754GumuzDibateKido192733628584754M61.2
BGDK-11H-56PRJEB39275SAMEA7050755GumuzDibateKido181206673544451F0.82
BGDK-12CPRJEB39275SAMEA7050756GumuzDibateKido173198494524249M0.84
BGDK-3CPRJEB39275SAMEA7050757GumuzDibateKido200476766604756M
BGDK-5H-82PRJEB39275SAMEA7050758GumuzDibateKido167630197504147F61.2
BGDK-6HPRJEB39275SAMEA7050759GumuzDibateKido206472010624758F
BGDK-7HPRJEB39275SAMEA7050760GumuzDibateKido202670391604457F
BGDK-8HPRJEB39275SAMEA7050761GumuzDibateKido177890612524050F
BGDK-9HPRJEB39275SAMEA7050762GumuzDibateKido172820697524249F0.6
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ODB-4H-002PRJEB39275SAMEA7050767OromiaDugdaBekele Girissa184572600554552F121.5
ODB-5HPRJEB39275SAMEA7050768OromiaDugdaBekele Girissa194734764584455F51
ODB-6C-093PRJEB39275SAMEA7050769OromiaDugdaBekele Girissa186013314564152M121
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ODB-8H-013PRJEB39275SAMEA7050771OromiaDugdaBekele Girissa184211704554252F51
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ODS-3CPRJEB39275SAMEA7050776OromiaDugdaShubi Gemo210036912635057M
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ODS-8H-042PRJEB39275SAMEA7050781OromiaDugdaShubi Gemo192840864584754F71.5
ODS-9H-016PRJEB39275SAMEA7050782OromiaDugdaShubi Gemo203753022614757F121
SDK-10C-004PRJEB39275SAMEA7050783SNNPRDaraKumato179621620544251M101
SDK-1H-080PRJEB39275SAMEA7050784SNNPRDaraKumato191383859574454F12
SDK-2CPRJEB39275SAMEA7050785SNNPRDaraKumato210686761634959M181.7
SDK-3H-054PRJEB39275SAMEA7050786SNNPRDaraKumato209572541635059F181.7
SDK-4C-062PRJEB39275SAMEA7050787SNNPRDaraKumato223374021675563M121.5
SDK-5HPRJEB39275SAMEA7050788SNNPRDaraKumato191841797564354F
SDK-6H-052PRJEB39275SAMEA7050789SNNPRDaraKumato187517459564653F121.5
SDK-7HPRJEB39275SAMEA7050790SNNPRDaraKumato205742068614858F121.6
SDK-8C-021PRJEB39275SAMEA7050791SNNPRDaraKumato210263073634959M121.6
SDK-9H-026PRJEB39275SAMEA7050792SNNPRDaraKumato190512885574754F101
SDL-10H-017PRJEB39275SAMEA7050793SNNPRDaraLoya218242387655361F71.5
SDL-1C-091PRJEB39275SAMEA7050794SNNPRDaraLoya494126576148123139M121.5
SDL-2H-064PRJEB39275SAMEA7050795SNNPRDaraLoya167570521504147F71.5
SDL-3C-019PRJEB39275SAMEA7050796SNNPRDaraLoya209340893635159M82
SDL-4H-066PRJEB39275SAMEA7050797SNNPRDaraLoya209633949634859F121
SDL-5H-008PRJEB39275SAMEA7050798SNNPRDaraLoya195060857584655F71
SDL-6H-057PRJEB39275SAMEA7050799SNNPRDaraLoya187214881564453F81
SDL-7C-035PRJEB39275SAMEA7050800SNNPRDaraLoya220419363665262F91.5
SDL-8C-090PRJEB39275SAMEA7050801SNNPRDaraLoya173775632524149M71
SDL-9H-013PRJEB39275SAMEA7050802SNNPRDaraLoya215730805645261F81.5
TGENF_110PRJEB39275SAMEA7050803TigrayEndertaMeseret256139496745672F251.25
TGENF_128PRJEB39275SAMEA7050804TigrayEndertaMeseret165845435483747F260.8
TGENF_134PRJEB39275SAMEA7050805TigrayEndertaMeseret203215770614857F251
TGENF_145PRJEB39275SAMEA7050806TigrayEndertaMeseret334654947997794F261.3
TGENF_177PRJEB39275SAMEA7050807TigrayEndertaMeseret158159539463545F280.85
TGENF_178PRJEB39275SAMEA7050808TigrayEndertaMeseret251142145735871F301.7
TGENM_135PRJEB39275SAMEA7050809TigrayEndertaMeseret177253135534150M281.55
TGENM_146PRJEB39275SAMEA7050810TigrayEndertaMeseret194712607584455M301.8
TGENM_150PRJEB39275SAMEA7050811TigrayEndertaMeseret199736461604556M261.45
TGENM_175PRJEB39275SAMEA7050812TigrayEndertaMeseret215840911634961M261.2
TMLHA_13HPRJEB39275SAMEA7050813TigrayMereblekeHadush Adi171655146514248F81.2
TMLHA-04CPRJEB39275SAMEA7050814TigrayMereblekeHadush Adi159294195483945M2.6
TMLHA-19HPRJEB39275SAMEA7050815TigrayMereblekeHadush Adi248627376745870F1.2
TMLHA-54HPRJEB39275SAMEA7050816TigrayMereblekeHadush Adi198560606584556F
TMLHA-66CPRJEB39275SAMEA7050817TigrayMereblekeHadush Adi456440319136107129M1.83
TMLHA-86HPRJEB39275SAMEA7050818TigrayMereblekeHadush Adi157424722473644F121.3
TMLHA-90CPRJEB39275SAMEA7050819TigrayMereblekeHadush Adi197521255584456M
TMLHA-91CPRJEB39275SAMEA7050820TigrayMereblekeHadush Adi166424117503747F1
TMLHA-96HPRJEB39275SAMEA7050821TigrayMereblekeHadush Adi156203276473644F101.43
TMLM-_C94PRJEB39275SAMEA7050822TigrayMereblekeMihquan162650188493846M121.45
TMLM-26CPRJEB39275SAMEA7050823TigrayMereblekeMihquan177855728523950M
TMLM-6HPRJEB39275SAMEA7050824TigrayMereblekeMihquan166357341504147F121.1
TMLM-C30PRJEB39275SAMEA7050825TigrayMereblekeMihquan148859908443642M122.1
TMLM-C89PRJEB39275SAMEA7050826TigrayMereblekeMihquan186763080564553M101.1
TMLM-H18PRJEB39275SAMEA7050827TigrayMereblekeMihquan174320520524249F121.65
TMLM-H53PRJEB39275SAMEA7050828TigrayMereblekeMihquan180324068544351F101.6
TMLM-H57PRJEB39275SAMEA7050829TigrayMereblekeMihquan145397265433341F101.1
TMLM-H72PRJEB39275SAMEA7050830TigrayMereblekeMihquan165668541503847F121.3
TMLM-H84PRJEB39275SAMEA7050831TigrayMereblekeMihquan169294406513948F121.57
TSSG-07HPRJEB39275SAMEA7050832TigraySahareti SamireGijet182631706554351F
TSSG-29HPRJEB39275SAMEA7050833TigraySahareti SamireGijet150096758453742F151.7
TSSG-37CPRJEB39275SAMEA7050834TigraySahareti SamireGijet227048103685264M91.5
TSSG-40HPRJEB39275SAMEA7050835TigraySahareti SamireGijet142314691433440F70.9
TSSG-43CPRJEB39275SAMEA7050836TigraySahareti SamireGijet174185407524249M151.2
TSSG-44CPRJEB39275SAMEA7050837TigraySahareti SamireGijet447119431134103126M61.4
TSSG-47HPRJEB39275SAMEA7050838TigraySahareti SamireGijet157567523473644F121.4
TSSG-48HPRJEB39275SAMEA7050839TigraySahareti SamireGijet319244953947590F
TSSG-49CPRJEB39275SAMEA7050840TigraySahareti SamireGijet167635858503947M51.7
TSSM-17CPRJEB39275SAMEA7050841TigraySahareti SamireMetkilimat162493989493946M61.2
TSSM-21HPRJEB39275SAMEA7050842TigraySahareti SamireMetkilimat157876144473644F60.9
TSSM-35HPRJEB39275SAMEA7050843TigraySahareti SamireMetkilimat158631341473945F71.6
TSSM-52CPRJEB39275SAMEA7050844TigraySahareti SamireMetkilimat163067895493846M81.5
TSSM-62HPRJEB39275SAMEA7050845TigraySahareti SamireMetkilimat172603563524249F61.3
TSSM-64HPRJEB39275SAMEA7050846TigraySahareti SamireMetkilimat192284955574654F121.2
TSSM-68CPRJEB39275SAMEA7050847TigraySahareti SamireMetkilimat156208128473844M61.7
TSSM-81HPRJEB39275SAMEA7050848TigraySahareti SamireMetkilimat158955463473645F81.6
TSSM-92HPRJEB39275SAMEA7050849TigraySahareti SamireMetkilimat175441722524149F101.2
TSSM-99CPRJEB39275SAMEA7050850TigraySahareti SamireMetkilimat190253350574354M81.3

Genomic DNA isolation and quality control

All the collected blood samples were processed for DNA extraction at the BecA-ILRI Hub facility, Nairobi, Kenya (http://hub.africabiosciences.org/) using the Qiagen DNeasy blood and tissue kit protocol (https://www.qiagen.com/ca/resources/download.aspx?id=63e22fd7-6eed-4bcb-8097-7ec77bcd4de6&lang=en). DNA concentration was evaluated by spectrophotometry (Thermo Scientific NanoDrop spectrophotometer 2000c) and the integrity of DNA was confirmed by agarose gel electrophoresis. The genomic DNA (gDNA) from each sample was then normalized to a final volume of 100 µl and final concentration of 50 ng/µl and was sent to Edinburgh Genomics, UK for whole genome sequencing (WGS). At Edinburgh Genomics, gDNA samples were re-evaluated for quantity and quality using an AATI Fragment Analyzer and the DNF-487 Standard Sensitivity Genomic DNA Analysis Kit https://www.agilent.com/cs/library/usermanuals/public/quick-guide-dnf-487-genomic-dna-kit-SD-AT000137.pdf. The AATI ProSize 2.0 software (https://dna.biotech.iastate.edu/fragmentanalyzer.html) provided a quantification value and a quality (integrity) score for each gDNA sample. Samples with a score >7 passed quality control. Based on the quantification results, gDNA samples were pre-normalised to fall within the acceptable range for library preparation.

Sequence library preparation and quality control

Next Generation sequencing libraries were prepared using Illumina SeqLab specific TruSeq Nano High Throughput Library preparation kits in conjunction with the Hamilton MicroLab STAR and Clarity LIMS X Edition. The normalized gDNA samples were sheared to a 450 bp mean insert size using a Covaris LE220 focused-ultrasonicator. The inserts were ligated with blunt ended, A-tailed, size selected TruSeq adapters and enriched using eight cycles of PCR amplification. The libraries were evaluated for mean peak size and quantity using the Caliper GX Touch with a HT DNA 1k/12 K/HI SENS LabChip and HT DNA HI SENS Reagent Kit. The libraries were normalised to 5 nM using the GX data and the actual concentration was established using a Roche LightCycler 480 and a Kapa Illumina Library Quantification kit and Standards (https://rochesequencingstore.com/wp-content/uploads/2017/10/KAPA-Lib-Quant-ILMN_9.17-IfU_1.pdf).

Sequencing

The libraries were denatured, and pooled in groups of eight for clustering and sequencing using a Hamilton MicroLab STAR with Genologics Clarity LIMS X Edition. Libraries were clustered onto HiSeqX Flow cells v2.5 on cBot2s and the clustered flow cells were transferred to a HiSeqX for sequencing using a HiSeqX Ten Reagent kit v2.5. Sequencing was performed in paired-end mode with read length of 150 bp.

Sequencing data processing, mapping and variant calling

Demultiplexing was performed using bcl2fastq (v2.17.1.14)[14], allowing a single mismatch when assigning reads to barcodes. Adapters (Read1: AGATCGGAAGAGCACACGTCTGAACTCCAGTCA, Read2: AGATCGGAAGA GCGTCGTGTAGGGAAAGAGTGT) were trimmed during the demultiplexing process. Sequencing data quality was checked using the FASTQC package (v0.11.5)[15]. FASTQC reports for all samples were aggregated in a single report by the MultiQC package[16] for easy review of sequence quality. No quality-based trimming was performed on the sequence reads prior to mapping and sequencing data from all samples were processed. Sequence reads were mapped against the latest version of chicken reference genome (GCA_000002315.5_GRCg6a) using the BWA-mem (v0.7.15) algorithm[17]. The resulting SAM/BAM files from the mapping step underwent a series of further processing steps, including coordinate sorting (using the SortSam function in Picard v2.9.2), duplicate reads marking (using MarkDuplicates function in Picard) and Base Quality Score Recalibration (BQSR) using GTAK v3.8-0. The final recalibrated BAM files were then used for variant calling. Figure 1 shows an overview of the mapping and variant calling steps. SNP calling was performed following the GATK best practice protocol for “Germline short variant discovery”[18] using the HaplotypeCaller function on individual samples followed by joint genotyping (using GenotypeGVCFs function) of the samples. Variant filtration was performed by applying the Variant Quality Score Recalibration (VQSR) approach[19] in GATK (v 3.8-0) using about one million validated SNPs[20] as a training and true set, and over 20 M known chicken SNPs from the Ensembl database as known variants. During the VQSR step the following annotations or context statistics were considered: read depth (DP), variant quality by depth (QD), root mean square of mapping quality (MQ), mapping quality rank sum test statistic (MQRankSum), read position rank sum test statistic (ReadPosRankSum), and strand bias statistics (FS and SOR). A tranche sensitivity threshold of 99% was applied for filtering variants. The “Code availability” section below shows the specific codes for each mapping and variant-calling step. As the final quality control of the called variants, any SNPs with a missing genotype rate of more than 20% across the samples were filtered out using VCFtools (option – max-missing 0.8).

Data Records

The raw full-length sequencing data (in FASTQ format) have been submitted to the European Nucleotide Archive (ENA) under the accession number PRJEB39275[13]. The VCF file of ~15 M SNPs detected from this dataset has been deposited in the European Variation Archive (EVA) with the accession number for Project: PRJEB46494[21] and Analyses: ERZ2899764.

Technical Validation

Quality control of sequencing data

For each sample, 41 Gb to 148 Gb sequencing yield (number of bases generated) was obtained, of which 74–83% of the bases (average 79%) had a minimum Phred scaled quality score of 30, indicating expected base calling accuracy of 99.9% (Fig. 2). The average estimated coverage for the samples varied from 38X to 139X (average across all samples 57X) (Fig. 2). Figure 3 shows selected features from FASTQC reports regarding sequencing quality (consolidated for all samples by the MultiQC package). This confirmed overall high quality sequencing data. Although Fig. 3b shows “Fails” signal for many reads, this should not be a matter of concern. All these “Fails” signals are associated with Read2 of the paired reads. Typically, Read2 often has a lower average quality than Read1[22]. A gradual drop in sequencing quality towards the end of the reads is also typical and expected of Illumina sequencing. It is important to note that Fig. 3d confirms a high average quality score for all reads. The mapping success rates of the sequence reads against the chicken reference genome were very high – 98.2% to 99.5% - which further confirmed the high quality of the sequencing data.
Fig. 2

Boxplots showing the distributions of sequencing yield, yield Q30 and estimated coverage for Ethiopian chicken samples (n = 234).

Fig. 3

Quality control metrics from FastQC analysis of sequencing data. The metrics from all sequence FASTQ files (total 540) are combined using the MultiQC package.

Boxplots showing the distributions of sequencing yield, yield Q30 and estimated coverage for Ethiopian chicken samples (n = 234). Quality control metrics from FastQC analysis of sequencing data. The metrics from all sequence FASTQ files (total 540) are combined using the MultiQC package.

Quality control of SNP data

Joint genotyping of all samples originally identified about 25 M SNPs. To ensure variant quality and minimize false positives, VQSR filtration was applied. By using machine learning algorithms, the VQSR method clusters the called variants based on annotation profiles of a set of known true positive SNPs (training set) in the detected set and calculates, for each variant, a new score called VQSLOD (https://gatk.broadinstitute.org/hc/en-us/articles/360035531612-Variant-Quality-Score-Recalibration-VQSR-). For filtration of the variants, we applied a VQSLOD threshold that retained 99% of the training variants. This filtration retained about 19 M SNPs. Further filtration based on missing genotypes (removed any SNPs with missing rate >20%) retained ~15 M good quality SNPs. About 86% of these variants have already been reported in the public databases. This provides extra confidence in the validity of the detected SNPs. Transition and transversion ratio (Ti/Tv) is used as a quality control metric for SNP calling. For whole genome sequencing data, the typical value is ~2[23]. A higher ratio generally indicates better SNP calling unless the ratio is too high (>4)[24]. We obtained a Ti/Tv ratio of 2.38 for 19 M SNPs after VQSR filtration and a ratio of 2.5 for the 15 M final set. Table 2 and the heat maps of SNP density across different chromosomes in Fig. 4 show a good representation of most chromosomes and regions except some microchromosomes (e.g., chr16, 22, 25, 30–33) and the sex chromosomes (Fig. 4). Chromosome 16 is known to have a high repeat content[25] whereas most microchromosomes have higher GC contents[26]; both causing difficulty in sequencing and mapping. The detected SNPs also had a good representation of different annotation categories in relation to their positions within or outside genes (Table 3).
Table 2

Summary statistics of SNPs in the VCF file for each chromosome.

ChromosomeGenBank accession of chromosome (as appears in the VCF)SNP countSNP density (count/kb)
1CM000093.52,928,34414.82
2CM000094.52,239,98914.96
3CM000095.51,661,03514.99
4CM000096.51,417,21315.52
5CM000097.5910,26415.22
6CM000098.5620,26017.05
7CM000099.5572,07415.57
8CM000100.5424,72614.05
9CM000101.5399,62616.55
10CM000102.5314,97814.91
11CM000103.5278,39113.78
12CM000104.5329,82516.18
13CM000105.5290,34915.15
14CM000106.5249,99715.41
15CM000107.5182,24513.95
16CM000108.57,9042.78
17CM000109.5164,25615.26
18CM000110.5184,13216.19
19CM000111.5155,99115.11
20CM000112.5219,72515.81
21CM000113.5108,59215.86
22CM000114.538,9437.13
23CM000115.595,10815.47
24CM000116.5105,19316.21
25CM000124.533,9758.54
26CM000117.593,98015.52
27CM000118.576,5409.48
28CM000119.577,75315.20
30CM003637.26,8253.75
31CM003638.28,6581.40
32CM000120.43,9875.49
33CM000123.535,8384.59
WCM000121.51080.02
ZCM000122.559,19047.17
unplaced7,210
Fig. 4

Chromosome-wise SNP distribution heat map across the Ethiopian indigenous chicken genomes based on 15 M SNPs. X-axis denotes the chromosome size in base pairs (bp) and Y-axis the chromosome number. The SNP count was calculated for 10 kb non-overlapping windows.

Table 3

SNPs in different annotation categories.

Annotation categoriescount% of total
exonic-nonsynonymous63,0080.425
exonic-synonymous140,6590.948
exonic-stopgain/loss7220.005
intronic6,867,83646.279
splicing4580.003
ncRNA_exonic145,9860.984
ncRNA_intronic1,413,2609.523
ncRNA_splicing8670.006
UTR3/UTR5159,0621.072
up/donwstream501,9013.382
intergenic5,546,21337.373
Total14,839,972
Summary statistics of SNPs in the VCF file for each chromosome. Chromosome-wise SNP distribution heat map across the Ethiopian indigenous chicken genomes based on 15 M SNPs. X-axis denotes the chromosome size in base pairs (bp) and Y-axis the chromosome number. The SNP count was calculated for 10 kb non-overlapping windows. SNPs in different annotation categories.
Measurement(s)genome
Technology Type(s)DNA sequencing
Factor Type(s)animal population
Sample Characteristic - OrganismGallus gallus
Sample Characteristic - LocationEthiopia
  15 in total

1.  Variant association tools for quality control and analysis of large-scale sequence and genotyping array data.

Authors:  Gao T Wang; Bo Peng; Suzanne M Leal
Journal:  Am J Hum Genet       Date:  2014-05-01       Impact factor: 11.025

2.  Genome measures used for quality control are dependent on gene function and ancestry.

Authors:  Jing Wang; Leon Raskin; David C Samuels; Yu Shyr; Yan Guo
Journal:  Bioinformatics       Date:  2014-10-08       Impact factor: 6.937

3.  Whole-genome resequencing reveals loci under selection during chicken domestication.

Authors:  Carl-Johan Rubin; Michael C Zody; Jonas Eriksson; Jennifer R S Meadows; Ellen Sherwood; Matthew T Webster; Lin Jiang; Max Ingman; Ted Sharpe; Sojeong Ka; Finn Hallböök; Francois Besnier; Orjan Carlborg; Bertrand Bed'hom; Michèle Tixier-Boichard; Per Jensen; Paul Siegel; Kerstin Lindblad-Toh; Leif Andersson
Journal:  Nature       Date:  2010-03-10       Impact factor: 49.962

4.  863 genomes reveal the origin and domestication of chicken.

Authors:  Ming-Shan Wang; Mukesh Thakur; Min-Sheng Peng; Yu Jiang; Laurent Alain François Frantz; Ming Li; Jin-Jin Zhang; Sheng Wang; Joris Peters; Newton Otieno Otecko; Chatmongkon Suwannapoom; Xing Guo; Zhu-Qing Zheng; Ali Esmailizadeh; Nalini Yasoda Hirimuthugoda; Hidayat Ashari; Sri Suladari; Moch Syamsul Arifin Zein; Szilvia Kusza; Saeed Sohrabi; Hamed Kharrati-Koopaee; Quan-Kuan Shen; Lin Zeng; Min-Min Yang; Ya-Jiang Wu; Xing-Yan Yang; Xue-Mei Lu; Xin-Zheng Jia; Qing-Hua Nie; Susan Joy Lamont; Emiliano Lasagna; Simone Ceccobelli; Humpita Gamaralalage Thilini Nisanka Gunwardana; Thilina Madusanka Senasige; Shao-Hong Feng; Jing-Fang Si; Hao Zhang; Jie-Qiong Jin; Ming-Li Li; Yan-Hu Liu; Hong-Man Chen; Cheng Ma; Shan-Shan Dai; Abul Kashem Fazlul Haque Bhuiyan; Muhammad Sajjad Khan; Gamamada Liyanage Lalanie Pradeepa Silva; Thi-Thuy Le; Okeyo Ally Mwai; Mohamed Nawaz Mohamed Ibrahim; Megan Supple; Beth Shapiro; Olivier Hanotte; Guojie Zhang; Greger Larson; Jian-Lin Han; Dong-Dong Wu; Ya-Ping Zhang
Journal:  Cell Res       Date:  2020-06-25       Impact factor: 25.617

5.  Functional classification of 15 million SNPs detected from diverse chicken populations.

Authors:  Almas A Gheyas; Clarissa Boschiero; Lel Eory; Hannah Ralph; Richard Kuo; John A Woolliams; David W Burt
Journal:  DNA Res       Date:  2015-04-29       Impact factor: 4.458

6.  MultiQC: summarize analysis results for multiple tools and samples in a single report.

Authors:  Philip Ewels; Måns Magnusson; Sverker Lundin; Max Käller
Journal:  Bioinformatics       Date:  2016-06-16       Impact factor: 6.937

7.  Genome diversity of Chinese indigenous chicken and the selective signatures in Chinese gamecock chicken.

Authors:  Wei Luo; Chenglong Luo; Meng Wang; Lijin Guo; Xiaolan Chen; Zhenhui Li; Ming Zheng; Bello Semiu Folaniyi; Wen Luo; Dingming Shu; Linliang Song; Meixia Fang; Xiquan Zhang; Hao Qu; Qinghua Nie
Journal:  Sci Rep       Date:  2020-09-03       Impact factor: 4.379

8.  The role of local adaptation in sustainable village chicken production.

Authors:  Judy M Bettridge; Androniki Psifidi; Zelalem G Terfa; Takele T Desta; Maria Lozano-Jaramillo; Tadelle Dessie; Pete Kaiser; Paul Wigley; Olivier Hanotte; Robert M Christley
Journal:  Nat Sustain       Date:  2018-10-15

9.  Deep landscape update of dispersed and tandem repeats in the genome model of the red jungle fowl, Gallus gallus, using a series of de novo investigating tools.

Authors:  Sébastien Guizard; Benoît Piégu; Peter Arensburger; Florian Guillou; Yves Bigot
Journal:  BMC Genomics       Date:  2016-08-19       Impact factor: 3.969

10.  Integrated Environmental and Genomic Analysis Reveals the Drivers of Local Adaptation in African Indigenous Chickens.

Authors:  Almas A Gheyas; Adriana Vallejo-Trujillo; Adebabay Kebede; Maria Lozano-Jaramillo; Tadelle Dessie; Jacqueline Smith; Olivier Hanotte
Journal:  Mol Biol Evol       Date:  2021-09-27       Impact factor: 16.240

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