Mosdepth: quick coverage calculation for genomes and exomes
暂无分享,去创建一个
[1] Yun S. Song,et al. The Simons Genome Diversity Project: 300 genomes from 142 diverse populations , 2016, Nature.
[2] Heng Li,et al. Toward better understanding of artifacts in variant calling from high-coverage samples , 2014, Bioinform..
[3] Aaron R. Quinlan,et al. BIOINFORMATICS APPLICATIONS NOTE , 2022 .
[4] Edwin Cuppen,et al. Sambamba: fast processing of NGS alignment formats , 2015, Bioinform..
[5] A. Quinlan. BEDTools: The Swiss‐Army Tool for Genome Feature Analysis , 2014, Current protocols in bioinformatics.
[6] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[7] Brent S. Pedersen,et al. Indexcov: fast coverage quality control for whole-genome sequencing , 2017, bioRxiv.
[8] S. Hochreiter,et al. cn.MOPS: mixture of Poissons for discovering copy number variations in next-generation sequencing data with a low false discovery rate , 2012, Nucleic acids research.