Results for "CNV"
Blogs
...his webinar, we will present clinical case studies in on Hereditary Breast and Ovarian Cancer (HBOC) and Retinoblastoma patients to demonstrate how CNV analysis in Strand NGS enable...2802 days ago
Structural variation: the hidden genomic treasure
...notyping and understanding of CNVs is lagging behind due to muc...s are copy number variations (CNVs) which can be generated by s...cting copy number variations (CNVs). These technologies have en...have been documented. Tools CNVnatora tool for CNV discovery...2701 days ago
Bookmarks
- ..., we recommend Google Chrome. BioCircos.js provides SNP, CNV, HEATMAP, LINK,&nbs...nd HISTGRAMmodules to display genome-wide genetic variations (SNPs, CNVs and chromosome rearrangement...
2296 days ago
mosdepth: fast BAM/CRAM depth calculation for WGS, exome, or targeted sequencing
...epth about 2x as fast samtools depth--about 25 minutes of CPU time for a 30X genome.mean per-window depth given a window size--as would be used for CNV calling.the mean per-region g...1630 days ago
Top-level pages
Commercial and public next-gen-seq (NGS) software
...Sciences Centre. Python/Win or Linux. Counting e.g. CHiP-Seq, Bis-Seq, CNV-Seq BS-Seq - The source code...Seq - Program used by Johnson et al. (2007) in their Science publication CNV-Seq - CNV-seq, a new method t...3517 days ago
Apps for Busy Bioinformatics Researchers !!!
...SS feeds for journals Query GeneRIF interactions, COSMIC mutations, and CNV data for cell lines. Does no...ntaining cell lines can be queried for mutations. Copy Number Variation (CNV) plots from cell lines profil...3540 days ago
- +3 more Top-level pages
ResearchLabs posts
- ...d mice. Research Area: Mapping loci in ENU mutants in mice in complex pedigrees Investigation of DNA sharing in distantly related individuals CNV analysis in pedigrees and con...
3946 days ago
Bio-Scripts
Create random 10000 SNPs in genome !
...21] Starting simuG .. [Sun Jan 10 16:05:57 2021] Check specified options .. Running simuG for SNP/INDEL simulation >> Ignore all options for CNV/inversion/translocation simul...1209 days ago
Create random 1000 INDEL in genome !
...21] Starting simuG .. [Sun Jan 10 16:14:00 2021] Check specified options .. Running simuG for SNP/INDEL simulation >> Ignore all options for CNV/inversion/translocation simul...1209 days ago
- +2 more Bio-Scripts
Tags
- EXCAVATOR2 is a collection of bash, R and Fortran scripts and codes that analyses Whole Exome Sequencing (WES) data to identify CNVs. EXCAVATOR2 enhances the identification of all genomic CNVs, both overlapping and non-overlapping targeted exons by integrating the analysis of In-targets and Off- ...
Tags: Bioinformatics, Analysis, CNV, EXCAVATOR2, tool, NGS
2711 days ago
Comments
Comment on "Does anyone have Nanopore latest updates?"
Nano conference https://publications.nanoporetech.com/2016/06/05/london-calling-talk-sara-goodwin-cshl-rapid-cnv-characterisation-of-clinical-cancer-samples-on-the-oxford-nanopore-minion/2888 days ago
