Biocview "ExomeSeq"

A Normalization and Copy Number Variation Detection Method for Whole Exome Sequencing
A Normalization and Copy Number Variation Detection Method for Whole Exome Sequencing
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
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.
Copy number information from targeted sequencing using off-target reads
Copy number information from targeted sequencing using off-target reads
Copy number information from targeted sequencing using off-target reads
Copy number information from targeted sequencing using off-target reads
Excluding host reads from xenograft sequencing data
Identification of cancer cell lines based on their weighted mutational or variational fingerprint
Identification of cancer cell lines based on their weighted mutational or variational fingerprint
Infers clonal composition of a tumor
Infers clonal composition of a tumor
NGScopy: Detection of Copy Number Variations in Next Generation Sequencing sequencing
NGScopy: Detection of Copy Number Variations in Next Generation Sequencing sequencing
Subclonal copy number and LOH prediction from whole genome sequencing of tumours
Subclonal copy number and LOH prediction from whole genome sequencing of tumours
Subclonal copy number and LOH prediction from whole genome sequencing of tumours
Testing for association between RNA-Seq and high-dimensional data
Testing for association between RNA-Seq and high-dimensional data
Testing for association between RNA-Seq and high-dimensional data