Topic: low-coverage-sequencing Goto Github
Some thing interesting about low-coverage-sequencing
Some thing interesting about low-coverage-sequencing
low-coverage-sequencing,Estimating tumor fraction in cell-free DNA from ultra-low-pass whole genome sequencing.
Organization: broadinstitute
low-coverage-sequencing,
Organization: green-lab-mdacc
low-coverage-sequencing,Two Nextflow pipelines for mapping and imputation of non-human samples sequenced at low-coverage.
User: maddalenacella
low-coverage-sequencing,LCVCFtools is a program designed for working with VCF files generated from low-coverage whole genome sequencing
User: marcusnizalvarez
low-coverage-sequencing,Supporting data for "Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients"
User: renatosantos98
low-coverage-sequencing,Asses the validity of imputation of your low-coverage samples
User: sonisarm
low-coverage-sequencing,Genotype imputation pipelines for the UK Biobank Research Analysis Platform
User: srubinacci
Home Page: https://srubinacci.gitbook.io/uk-biobank-imputation-pipelines/
low-coverage-sequencing,The repo was not under development. Check out angsd toolkit for low depth data analyses.
User: zilong-li
Home Page: https://www.popgen.dk/angsd/index.php/SNP_calling
low-coverage-sequencing,Imputation workflow for low coverage whole genome sequencing data
User: zilong-li
low-coverage-sequencing,Imputation and Admixture for lcWGS in one goal
User: zilong-li
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