Identifying genomic regions with high quality single nucleotide variant calling
Population Based Metrics to Stratify Somatic Variant Calling Performance
HiC-Pro: an optimized and flexible pipeline for Hi-C data processing | Genome Biology | Full Text
HTSeq Reference Alignment Lab
Aug2013 illumina platinum genomes
Evaluating Somatic Variant Calling in Tumor/Normal Studies
Optimizing Cancer Genome Sequencing and Analysis - ScienceDirect
System analysis of the sequencing quality of human whole exome samples on BGI NGS platform | Scientific Reports
Aug2013 illumina platinum genomes
Hybrid Genome in a Bottle and Platinum Genomes truthset The hybrid... | Download Scientific Diagram
Aug2013 illumina platinum genomes
Elliott Margulies - Striving for Perfection: The Platinum Genomes Project
Identifying genomic regions with high quality single nucleotide variant calling
A diploid assembly-based benchmark for variants in the major histocompatibility complex | Nature Communications
Identifying genomic regions with high quality single nucleotide variant calling
Allele-specific analysis. a Allele-specific analysis of the GM12878... | Download Scientific Diagram
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease | npj Genomic Medicine
the results obtained on Platinum Genome NA12877. The compression and... | Download Scientific Diagram
Accuracy and efficiency of germline variant calling pipelines for human genome data | Scientific Reports
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios
genomicsnotebook/genomics-platinum-genomes.ipynb at main · microsoft/genomicsnotebook · GitHub
Longshot enables accurate variant calling in diploid genomes from single-molecule long read sequencing | Nature Communications
Reproducible integration of multiple sequencing datasets to form high-confidence SNP, indel, and reference calls for five human genome reference materials | bioRxiv
