Literature DB >> 26963554

Haplotypes drop by drop.

Jacob O Kitzman1.   

Abstract

Mesh:

Year:  2016        PMID: 26963554     DOI: 10.1038/nbt.3500

Source DB:  PubMed          Journal:  Nat Biotechnol        ISSN: 1087-0156            Impact factor:   54.908


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  12 in total

1.  Noninvasive whole-genome sequencing of a human fetus.

Authors:  Jacob O Kitzman; Matthew W Snyder; Mario Ventura; Alexandra P Lewis; Ruolan Qiu; Lavone E Simmons; Hilary S Gammill; Craig E Rubens; Donna A Santillan; Jeffrey C Murray; Holly K Tabor; Michael J Bamshad; Evan E Eichler; Jay Shendure
Journal:  Sci Transl Med       Date:  2012-06-06       Impact factor: 17.956

2.  Droplet barcoding for single-cell transcriptomics applied to embryonic stem cells.

Authors:  Allon M Klein; Linas Mazutis; Ilke Akartuna; Naren Tallapragada; Adrian Veres; Victor Li; Leonid Peshkin; David A Weitz; Marc W Kirschner
Journal:  Cell       Date:  2015-05-21       Impact factor: 41.582

Review 3.  Haplotype-resolved genome sequencing: experimental methods and applications.

Authors:  Matthew W Snyder; Andrew Adey; Jacob O Kitzman; Jay Shendure
Journal:  Nat Rev Genet       Date:  2015-05-07       Impact factor: 53.242

Review 4.  Haplotype phasing: existing methods and new developments.

Authors:  Sharon R Browning; Brian L Browning
Journal:  Nat Rev Genet       Date:  2011-09-16       Impact factor: 53.242

Review 5.  The importance of phase information for human genomics.

Authors:  Ryan Tewhey; Vikas Bansal; Ali Torkamani; Eric J Topol; Nicholas J Schork
Journal:  Nat Rev Genet       Date:  2011-02-08       Impact factor: 53.242

6.  Haplotype-resolved genome sequencing of a Gujarati Indian individual.

Authors:  Jacob O Kitzman; Alexandra P Mackenzie; Andrew Adey; Joseph B Hiatt; Rupali P Patwardhan; Peter H Sudmant; Sarah B Ng; Can Alkan; Ruolan Qiu; Evan E Eichler; Jay Shendure
Journal:  Nat Biotechnol       Date:  2010-12-19       Impact factor: 54.908

7.  Resolving the complexity of the human genome using single-molecule sequencing.

Authors:  Mark J P Chaisson; John Huddleston; Megan Y Dennis; Peter H Sudmant; Maika Malig; Fereydoun Hormozdiari; Francesca Antonacci; Urvashi Surti; Richard Sandstrom; Matthew Boitano; Jane M Landolin; John A Stamatoyannopoulos; Michael W Hunkapiller; Jonas Korlach; Evan E Eichler
Journal:  Nature       Date:  2014-11-10       Impact factor: 49.962

8.  Non-invasive prenatal measurement of the fetal genome.

Authors:  H Christina Fan; Wei Gu; Jianbin Wang; Yair J Blumenfeld; Yasser Y El-Sayed; Stephen R Quake
Journal:  Nature       Date:  2012-07-19       Impact factor: 49.962

9.  Massive genomic rearrangement acquired in a single catastrophic event during cancer development.

Authors:  Philip J Stephens; Chris D Greenman; Beiyuan Fu; Fengtang Yang; Graham R Bignell; Laura J Mudie; Erin D Pleasance; King Wai Lau; David Beare; Lucy A Stebbings; Stuart McLaren; Meng-Lay Lin; David J McBride; Ignacio Varela; Serena Nik-Zainal; Catherine Leroy; Mingming Jia; Andrew Menzies; Adam P Butler; Jon W Teague; Michael A Quail; John Burton; Harold Swerdlow; Nigel P Carter; Laura A Morsberger; Christine Iacobuzio-Donahue; George A Follows; Anthony R Green; Adrienne M Flanagan; Michael R Stratton; P Andrew Futreal; Peter J Campbell
Journal:  Cell       Date:  2011-01-07       Impact factor: 41.582

10.  Synthetic long-read sequencing reveals intraspecies diversity in the human microbiome.

Authors:  Volodymyr Kuleshov; Chao Jiang; Wenyu Zhou; Fereshteh Jahanbani; Serafim Batzoglou; Michael Snyder
Journal:  Nat Biotechnol       Date:  2015-12-14       Impact factor: 54.908

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  11 in total

Review 1.  The frontiers of sequencing in undiagnosed neurodevelopmental diseases.

Authors:  Hane Lee; Stanley F Nelson
Journal:  Curr Opin Genet Dev       Date:  2020-06-27       Impact factor: 5.578

2.  Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis.

Authors:  Se Song Jang; Byung Chan Lim; Seong-Keun Yoo; Jong-Yeon Shin; Ki-Joong Kim; Jeong-Sun Seo; Jong-Il Kim; Jong Hee Chae
Journal:  Sci Rep       Date:  2018-06-06       Impact factor: 4.379

Review 3.  An Introduction to the Analysis of Single-Cell RNA-Sequencing Data.

Authors:  Aisha A AlJanahi; Mark Danielsen; Cynthia E Dunbar
Journal:  Mol Ther Methods Clin Dev       Date:  2018-08-02       Impact factor: 6.698

4.  Indel-correcting DNA barcodes for high-throughput sequencing.

Authors:  John A Hawkins; Stephen K Jones; Ilya J Finkelstein; William H Press
Journal:  Proc Natl Acad Sci U S A       Date:  2018-06-20       Impact factor: 11.205

5.  Divide and conquer: A perspective on biochips for single-cell and rare-molecule analysis by next-generation sequencing.

Authors:  A C Lee; Y Lee; D Lee; S Kwon
Journal:  APL Bioeng       Date:  2019-06-25

Review 6.  The Current State of Cephalopod Science and Perspectives on the Most Critical Challenges Ahead From Three Early-Career Researchers.

Authors:  Caitlin E O'Brien; Katina Roumbedakis; Inger E Winkelmann
Journal:  Front Physiol       Date:  2018-06-06       Impact factor: 4.566

7.  Alternative splicing signatures in preimplantation embryo development.

Authors:  Geng G Tian; Jing Li; Ji Wu
Journal:  Cell Biosci       Date:  2020-03-10       Impact factor: 7.133

8.  De novo assembly of the olive fruit fly (Bactrocera oleae) genome with linked-reads and long-read technologies minimizes gaps and provides exceptional Y chromosome assembly.

Authors:  Anthony Bayega; Haig Djambazian; Konstantina T Tsoumani; Maria-Eleni Gregoriou; Efthimia Sagri; Eleni Drosopoulou; Penelope Mavragani-Tsipidou; Kristina Giorda; George Tsiamis; Kostas Bourtzis; Spyridon Oikonomopoulos; Ken Dewar; Deanna M Church; Alexie Papanicolaou; Kostas D Mathiopoulos; Jiannis Ragoussis
Journal:  BMC Genomics       Date:  2020-03-30       Impact factor: 3.969

9.  Single-cell transcriptomic atlas of the human retina identifies cell types associated with age-related macular degeneration.

Authors:  Madhvi Menon; Shahin Mohammadi; Jose Davila-Velderrain; Brittany A Goods; Tanina D Cadwell; Yu Xing; Anat Stemmer-Rachamimov; Alex K Shalek; John Christopher Love; Manolis Kellis; Brian P Hafler
Journal:  Nat Commun       Date:  2019-10-25       Impact factor: 14.919

10.  Haplotyping by linked-read sequencing (HLRS) of the genetic disease carriers for preimplantation genetic testing without a proband or relatives.

Authors:  Qing Li; Yan Mao; Shaoying Li; Hongzi Du; Wenzhi He; Jianchun He; Lingyin Kong; Jun Zhang; Bo Liang; Jianqiao Liu
Journal:  BMC Med Genomics       Date:  2020-08-20       Impact factor: 3.063

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