Results for "Chittaranjan National Cancer Institute"
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SATSUMA : Highly sensitive whole-genome synteny alignments.
Satsuma is a whole-genome synteny alignment program. It takes two genomes, computes...source code from here. Stable versions can also be downloaded from the Broad Institute's web site. An incomplete li...2927 days ago
- Tools for making blobplots or Taxon-Annotated-GC-Coverage plots (TAGC plots) to visualise the contents of genome assembly data sets as a QC step Blaxter Lab, Institute of Evolutionary Biology, Univ...
2896 days ago
AutoDock Vina: an open-source program for doing molecular docking.
AutoDock Vina is an open-source program for doing molecular docking. It was des...bsp;Dr. Oleg Trott in the Molecular Graphics Lab at The Scripps Research Institute. It is especially effect...1435 days ago
- The Sybil software package provides a primarily web-based...developed by the bioinformatics department at The Institute for Genomic Research (TIGR) and development continues at the J. Craig Venter Institute (JCVI) and the Institute for...
2810 days ago
- The accurate description and annotation of structural variants can be complex. This is due to the different...menclature recommendations [http://www.hgvs.org/rec.html]. http://cancer.sa...
2785 days ago
- Development of cancer is driven by somatic alterations, including numerical and structural chromosomal aberrations. Currently, several computational methods are availabl...
2167 days ago
- Visualization has played an extremely important role in the current genomic revolution..., here we show a gene fusion in the SK-BR-3 breast cancer cell line linking the genes C...e two genes (Figure 1a). More gene fusions of this cancer ce...
2766 days ago
- Seven Bridges is the biomedical data analysis company accelerating breakthroughs in genomics research for cancer, d...
2759 days ago
- Spines is a collection of software tools, developed and used by the Vertebrate Genome Biology Group at the Broad Institute. It provides basic data struc...
2728 days ago
- EXCAVATOR2 is a collection of bash, R and Fortran scripts and codes that analyses Whole Exome Sequencing (WES) dat...fication of CNVs in small as well as large-scale re-sequencing population and cancer st...
2726 days ago
