Literature DB >> 25641221

AftrRAD: a pipeline for accurate and efficient de novo assembly of RADseq data.

Michael G Sovic1,2, Anthony C Fries1, H Lisle Gibbs1,2.   

Abstract

An increase in studies using restriction site-associated DNA sequencing (RADseq) methods has led to a need for both the development and assessment of novel bioinformatic tools that aid in the generation and analysis of these data. Here, we report the availability of AftrRAD, a bioinformatic pipeline that efficiently assembles and genotypes RADseq data, and outputs these data in various formats for downstream analyses. We use simulated and experimental data sets to evaluate AftrRAD's ability to perform accurate de novo assembly of loci, and we compare its performance with two other commonly used programs, stacks and pyrad. We demonstrate that AftrRAD is able to accurately assemble loci, while accounting for indel variation among alleles, in a more computationally efficient manner than currently available programs. AftrRAD run times are not strongly affected by the number of samples in the data set, making this program a useful tool when multicore systems are not available for parallel processing, or when data sets include large numbers of samples.
© 2015 John Wiley & Sons Ltd.

Keywords:  RADseq; bioinformatics; de novo assembly; genotyping; locus identification

Mesh:

Year:  2015        PMID: 25641221     DOI: 10.1111/1755-0998.12378

Source DB:  PubMed          Journal:  Mol Ecol Resour        ISSN: 1755-098X            Impact factor:   7.090


  8 in total

1.  Deriving genotypes from RAD-seq short-read data using Stacks.

Authors:  Nicolas C Rochette; Julian M Catchen
Journal:  Nat Protoc       Date:  2017-11-30       Impact factor: 13.491

2.  Origin of a cryptic lineage in a threatened reptile through isolation and historical hybridization.

Authors:  M G Sovic; A C Fries; H L Gibbs
Journal:  Heredity (Edinb)       Date:  2016-07-27       Impact factor: 3.821

3.  Similarity thresholds used in DNA sequence assembly from short reads can reduce the comparability of population histories across species.

Authors:  Michael G Harvey; Caroline Duffie Judy; Glenn F Seeholzer; James M Maley; Gary R Graves; Robb T Brumfield
Journal:  PeerJ       Date:  2015-04-21       Impact factor: 2.984

4.  Selecting RAD-Seq Data Analysis Parameters for Population Genetics: The More the Better?

Authors:  Natalia Díaz-Arce; Naiara Rodríguez-Ezpeleta
Journal:  Front Genet       Date:  2019-05-29       Impact factor: 4.599

5.  Low impact of different SNP panels from two building-loci pipelines on RAD-Seq population genomic metrics: case study on five diverse aquatic species.

Authors:  Adrián Casanova; Francesco Maroso; Andrés Blanco; Miguel Hermida; Néstor Ríos; Graciela García; Alice Manuzzi; Lorenzo Zane; Ana Verissimo; José-Luís García-Marín; Carmen Bouza; Manuel Vera; Paulino Martínez
Journal:  BMC Genomics       Date:  2021-03-02       Impact factor: 3.969

6.  Hybrid origin of European Vipers (Vipera magnifica and Vipera orlovi) from the Caucasus determined using genomic scale DNA markers.

Authors:  Oleksandr Zinenko; Michael Sovic; Ulrich Joger; H Lisle Gibbs
Journal:  BMC Evol Biol       Date:  2016-04-12       Impact factor: 3.260

7.  Genetic diversity in migratory bats: Results from RADseq data for three tree bat species at an Ohio windfarm.

Authors:  Michael G Sovic; Bryan C Carstens; H Lisle Gibbs
Journal:  PeerJ       Date:  2016-01-26       Impact factor: 2.984

8.  2b-RAD genotyping for population genomic studies of Chagas disease vectors: Rhodnius ecuadoriensis in Ecuador.

Authors:  Luis E Hernandez-Castro; Marta Paterno; Anita G Villacís; Björn Andersson; Jaime A Costales; Michele De Noia; Sofía Ocaña-Mayorga; Cesar A Yumiseva; Mario J Grijalva; Martin S Llewellyn
Journal:  PLoS Negl Trop Dis       Date:  2017-07-19
  8 in total

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