Literature DB >> 33693500

Megadepth: efficient coverage quantification for BigWigs and BAMs.

Christopher Wilks1, Omar Ahmed1, Daniel N Baker1, David Zhang1,2,3,4, Leonardo Collado-Torres5, Ben Langmead1.   

Abstract

MOTIVATION: A common way to summarize sequencing datasets is to quantify data lying within genes or other genomic intervals. This can be slow and can require different tools for different input file types.
RESULTS: Megadepth is a fast tool for quantifying alignments and coverage for BigWig and BAM/CRAM input files, using substantially less memory than the next-fastest competitor. Megadepth can summarize coverage within all disjoint intervals of the Gencode V35 gene annotation for more than 19,000 GTExV8 BigWig files in approximately one hour using 32 threads. Megadepth is available both as a command-line tool and as an R/Bioconductor package providing much faster quantification compared to the rtracklayer package. AVAILABILITY: https://github.com/ChristopherWilks/megadepth,https://bioconductor.org/packages/megadepth.
© The Author(s) 2021. Published by Oxford University Press.

Entities:  

Year:  2021        PMID: 33693500     DOI: 10.1093/bioinformatics/btab152

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  4 in total

1.  Structural variant-based pangenome construction has low sensitivity to variability of haplotype-resolved bovine assemblies.

Authors:  Alexander S Leonard; Danang Crysnanto; Zih-Hua Fang; Michael P Heaton; Brian L Vander Ley; Carolina Herrera; Heinrich Bollwein; Derek M Bickhart; Kristen L Kuhn; Timothy P L Smith; Benjamin D Rosen; Hubert Pausch
Journal:  Nat Commun       Date:  2022-05-31       Impact factor: 17.694

2.  recount3: summaries and queries for large-scale RNA-seq expression and splicing.

Authors:  Christopher Wilks; Shijie C Zheng; Feng Yong Chen; Rone Charles; Brad Solomon; Jonathan P Ling; Eddie Luidy Imada; David Zhang; Lance Joseph; Jeffrey T Leek; Andrew E Jaffe; Abhinav Nellore; Leonardo Collado-Torres; Kasper D Hansen; Ben Langmead
Journal:  Genome Biol       Date:  2021-11-29       Impact factor: 13.583

3.  BamToCov, an efficient toolkit for sequence coverage calculations.

Authors:  Giovanni Birolo; Andrea Telatin
Journal:  Bioinformatics       Date:  2022-02-23       Impact factor: 6.931

4.  Direct long-read RNA sequencing identifies a subset of questionable exitrons likely arising from reverse transcription artifacts.

Authors:  Laura Schulz; Manuel Torres-Diz; Mariela Cortés-López; Katharina E Hayer; Mukta Asnani; Sarah K Tasian; Yoseph Barash; Elena Sotillo; Kathi Zarnack; Julian König; Andrei Thomas-Tikhonenko
Journal:  Genome Biol       Date:  2021-06-28       Impact factor: 13.583

  4 in total

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