2021
DOI: 10.1093/molbev/msab113
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The Pop-Gen Pipeline Platform: A Software Platform for Population Genomic Analyses

Abstract: The Pop-Gen Pipeline Platform (PPP) is a software platform for population genomic analyses. The PPP was designed as a collection of scripts that facilitate common population genomic workflows in a consistent and standardized Python environment. Functions were developed to encompass entire workflows, including: input preparation, file format conversion, various population genomic analyses, and output generation. The platform has also been developed with reproducibility and extensibility of analyses in mind. The… Show more

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Cited by 14 publications
(11 citation statements)
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“…To test for potential significant differences in genome-wide heterozygosity between the three cohorts, an ANOVA test was conducted. A fSFS was generated using the “ vcf_to_sfs ” tool distributed within the popgen pipeline platform ( Webb et al 2021 ).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…To test for potential significant differences in genome-wide heterozygosity between the three cohorts, an ANOVA test was conducted. A fSFS was generated using the “ vcf_to_sfs ” tool distributed within the popgen pipeline platform ( Webb et al 2021 ).…”
Section: Methodsmentioning
confidence: 99%
“…Afterwards, demographic changes were applied as depicted in supplementary figure S3 A – H , Supplementary Material online and a number of individuals were sampled equal to the number of fin whale individuals. fSFS were extracted from the resulting vcf files using the “ vcf_to_sfs ” tool as described above ( Webb et al 2021 ). Eventually, we compared different demographic simulations by calculating log-likelihoods of observing the empirical fSFS given one of the simulated fSFS using the R base function “ dmultinom ” ( supplementary table S4, Supplementary Material online).…”
Section: Methodsmentioning
confidence: 99%
“…Prior to population genomic analyses, further filtering was applied using BCFtools v.1.11 to remove (a) the sites that were not in Hardy–Weinberg equilibrium ( P < 10 −4 ) for analyses of population structure, genetic diversity, and estimates of contemporary and historic migration and (b) the sites in linkage disequilibrium ( R 2 > 0.6 in 1000 sites) that were filtered for F ST outlier analyses. All population genomics analyses were performed with the PPP pipeline [ 94 ] using the BCFtools v.1.11 ( https://samtools.github.io/bcftools/bcftools.html ).…”
Section: Methodsmentioning
confidence: 99%
“…The reads that aligned to mitochondrial (MT) genome-extracted from the WGS dataset using the Paleomix pipeline (see above for details)-were used in haplotype and variant calling (GATK v. Phylogenetic analyses were made in order to look at clustering of maternal linages. To reconstruct the phylogeny of mitochondrial protein coding genes (PCGs), fasta sequences were extracted from the VCF using PPP v0.1.12 (Webb et al, 2021). PCGs were extracted using BLASTN (Camacho et al, 2009), aligned with MAFFT v7.480 (Katoh & Standley, 2013), manually corrected for length, and ND6 was reverse complemented as it is encoded on the light strand.…”
Section: Mt Genome Analysesmentioning
confidence: 99%