Biocview "ExomeSeq"

A Normalization and Copy Number Variation Detection Method for Whole Exome Sequencing

Bias Awared Peak Calling and Quantification for MeRIP-Seq

Clonal ordering and visualization

Clone Identification from Single Cell Data

coMET: visualisation of regional epigenome-wide association scan (EWAS) results and DNA co-methylation patterns

coMET: visualisation of regional epigenome-wide association scan (EWAS) results and DNA co-methylation patterns.

Computes estimates of the probability of related individuals sharing a rare variant

Copy number information from ChIP_seq using off-target reads off-target reads

Copy number information from targeted sequencing using off-target reads

Excluding host reads from xenograft sequencing data

Global Test for Counts

Identification of cancer cell lines based on their weighted mutational/ variational fingerprint

Infers clonal composition of a tumor

Integrated Copy Number Variation detection

NGScopy: Detection of Copy Number Variations in Next Generation Sequencing sequencing

Subclonal copy number and LOH prediction from whole genome sequencing of tumours