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...2794 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...2693 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...
2288 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...1622 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...3509 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...3532 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...
3938 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...1201 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...1201 days ago
- +2 more Bio-Scripts
Tags
- The bakers yeast, Saccharomyces cerevisiae is an ideal model organism to understand mechanisms of meiotic chromosome segregation. In S. cerevisiae and in mammals, the majority of meiotic crossovers are formed through a highly conserved MSH4p-MSH5p, MLH1p-MLH3p dependent pathway. We are interested...
Tags: Bioinformatics, CrossOver, Recombination, Gene, Function, Genome, NGS, Sequences, CNV, Selection
2972 days ago
- TheLab seek to understand the genetic factors contributing to genomic variation and phenotypic diversity. To this end, we employ molecular and bioinformatic tools to study evolutionary processes at the level of populations, both experimental and natural, and genomes. Our research interests enco...
Tags: Bioinformatics, Duplication, Genome, Gene, Function, Population, NGS, Sequences, CNV, Selection
2982 days ago
- +1 more Tags
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/2881 days ago
