Estimating genotype error rates from high-coverage next-generation sequence data. Read more about Estimating genotype error rates from high-coverage next-generation sequence data.
DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly. Read more about DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly.
OutKnocker: a web tool for rapid and simple genotyping of designer nuclease edited cell lines. Read more about OutKnocker: a web tool for rapid and simple genotyping of designer nuclease edited cell lines.
Unbiased analysis of potential targets of breast cancer susceptibility loci by Capture Hi-C. Read more about Unbiased analysis of potential targets of breast cancer susceptibility loci by Capture Hi-C.
Seamless gene correction of β-thalassemia mutations in patient-specific iPSCs using CRISPR/Cas9 and piggyBac. Read more about Seamless gene correction of β-thalassemia mutations in patient-specific iPSCs using CRISPR/Cas9 and piggyBac.
Extensive and coordinated control of allele-specific expression by both transcription and translation in Candida albicans. Read more about Extensive and coordinated control of allele-specific expression by both transcription and translation in Candida albicans.
Recurrent epimutations activate gene body promoters in primary glioblastoma. Read more about Recurrent epimutations activate gene body promoters in primary glioblastoma.
Functional DNA methylation differences between tissues, cell types, and across individuals discovered using the M&M algorithm. Read more about Functional DNA methylation differences between tissues, cell types, and across individuals discovered using the M&M algorithm.
Estimating absolute methylation levels at single-CpG resolution from methylation enrichment and restriction enzyme sequencing methods. Read more about Estimating absolute methylation levels at single-CpG resolution from methylation enrichment and restriction enzyme sequencing methods.
Spark: a navigational paradigm for genomic data exploration. Read more about Spark: a navigational paradigm for genomic data exploration.
