2018
DOI: 10.1177/1176934317742613
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HybPhyloMaker: Target Enrichment Data Analysis From Raw Reads to Species Trees

Abstract: Summary:Hybridization-based target enrichment in combination with genome skimming (Hyb-Seq) is becoming a standard method of phylogenomics. We developed HybPhyloMaker, a bioinformatics pipeline that performs target enrichment data analysis from raw reads to supermatrix-, supertree-, and multispecies coalescent-based species tree reconstruction. HybPhyloMaker is written in BASH and integrates common bioinformatics tools. It can be launched both locally and on a high-performance computer cluster. Compared with e… Show more

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Cited by 49 publications
(41 citation statements)
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References 49 publications
(54 reference statements)
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“…Two different paired-end sequencing runs (2x 250 bp) were performed on an Illumina MiSeq System (Illumina Inc., San Diego, USA). The obtained raw reads were processed using the pipeline HybPhyloMaker (all scripts available at: https://github.com/tomas-fer/HybPhyloMaker/; Fér and Schmickl (2018). Before analyses, reads were phased using SAMtools vers.…”
Section: Methodsmentioning
confidence: 99%
“…Two different paired-end sequencing runs (2x 250 bp) were performed on an Illumina MiSeq System (Illumina Inc., San Diego, USA). The obtained raw reads were processed using the pipeline HybPhyloMaker (all scripts available at: https://github.com/tomas-fer/HybPhyloMaker/; Fér and Schmickl (2018). Before analyses, reads were phased using SAMtools vers.…”
Section: Methodsmentioning
confidence: 99%
“…for the pipeline with details of data preparation and analyses. A combination of HybPhyloMaker (Fér and Schmickl, ) and HybPiper (Johnson et al., ) was used for data preparation and analyses in the following sections. The first steps in data preparation for each sample were conducted in HybPhyloMaker, a pipeline that makes use of already available software (see details below) to perform Hyb‐Seq data analyses.…”
Section: Methodsmentioning
confidence: 99%
“…). The single reference file for read mapping in HybPiper contained all reference sequences for each of the 1061 reference loci; read mapping was conducted using BWA, and contig assembly was performed using SPAdes in HybPiper (see Fér and Schmickl [] for further comparisons between HybPiper and HybPhyloMaker). Paralogous loci were flagged in HybPiper using the following (default) settings: multiple long‐length contigs (>85% of the reference locus) with similar coverage (within 10× of each other) that mapped to a reference locus.…”
Section: Methodsmentioning
confidence: 99%
“…Lemmon & Lemmon, ; Barrett et al ., ) and generally demands less complex bioinformatics (e.g. Fér & Schmickl, ). Reduced representation techniques such as restriction site‐associated DNA sequencing (RADseq, Baird et al ., ) or genotype‐by‐sequencing (Elshire et al ., ) work well for population‐level analysis and do not require a reference genome.…”
Section: Introductionmentioning
confidence: 99%