Isaac, the Illumina variant calling workflow
暂无分享,去创建一个
Oliver Hofmann | Zachary D. Stephens | Gloria Rendon | Liudmila Sergeevna Mainzer | Brad Chapman | Victor Jongeneel | Z. Stephens | B. Chapman | G. Rendon | V. Jongeneel | L. S. Mainzer | Oliver M. Hofmann
[1] H. Hakonarson,et al. Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing , 2013, Genome Medicine.
[2] Ming Yi,et al. Performance comparison of SNP detection tools with illumina exome sequencing data—an assessment using both family pedigree information and sample-matched SNP array data , 2014, Nucleic acids research.
[3] Vineet Bafna,et al. Wessim: a whole-exome sequencing simulator based on in silico exome capture , 2013, Bioinform..
[4] Michael R. Speicher,et al. A survey of tools for variant analysis of next-generation genome sequencing data , 2013, Briefings Bioinform..
[5] Xiaoqing Yu,et al. Comparing a few SNP calling algorithms using low-coverage sequencing data , 2013, BMC Bioinformatics.
[6] Chittibabu Guda,et al. A Comparison of Variant Calling Pipelines Using Genome in a Bottle as a Reference , 2015, BioMed research international.
[7] Richard Durbin,et al. Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .