Jit
Enthusiast computational biologist with business dream !!!
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Porechop: tool for finding and removing adapters from Oxford Nanopore reads
By Rahul Nayak 2372 days agogithub.com - Porechop is a tool for finding and removing adapters from Oxford Nanopore reads. Adapters on the ends of reads are trimmed off, and when a read has an adapter in its middle, it is treated as chimeric and chopped into separate reads. Porechop...Walk-ins for JRF ans SRF post in NIRRH, Mumbai
Title of project- "EXPLORING THE HINGE AND TRANSMEMBRANE REGION OF HUMAN FSHR FOR DESIGN OF SMALL MOLECULE AND PEPTIDOMIMETIC MODULATORS" Name of the Post- Junior Research Fellow No. of vacancy- One Stipend- Rs. 25000/ +30% HRA Essential...RNA-seq Analysis Workshop Course Materials
By Jit 2337 days agochagall.med.cornell.edu - RNAseq can be roughly divided into two "types": Reference genome-based - an assembled genome exists for a species for which an RNAseq experiment is performed. It allows reads to be aligned against the reference genome and significantly improves...JRF Bioinformatics @ Pune University
Pune University is inviting applications from indian citizens for recruiting following posts: Vacancies: Junior Research Fellow-04 Age Limits: Candidates age should be not more than 28 years. Qualification: Candidates should possess M.Sc in...AlignQC: A tool for assessing an alignment, and generating reports that are easy to share
By Jit 2302 days agowww.healthcare.uiowa.edu - Long read alignment analysis. Generate a reports on sequence alignments for mappability vs read sizes, error patterns, annotations and rarefraction curve analysis. The most basic analysis only requires a BAM file, and outputs a web browser...Affy has acquired Eureka Genomics for 15M $
By Martin Jones 3477 days agoAffymetrix Acquires Assets Of Eureka Genomics CorporationPlatypus: A Haplotype-Based Variant Caller For Next Generation Sequence Data
By Shruti Paniwala 2223 days agowww.well.ox.ac.uk - Platypus is a tool designed for efficient and accurate variant-detection in high-throughput sequencing data. By using local realignment of reads and local assembly it achieves both high sensitivity and high specificity. Platypus can detect...Alessandra Carbone Lab
Our group works on various problems connected with the functioning and evolution of biological systems. We use mathematical tools, coming from statistics and combinatorics, algorithmic tools and molecular physics tools to study basic principles of...snakepipes: A toolkit based on snakemake and python for analysis of NGS data
By Jit 2006 days agogithub.com - snakePipes are flexible and powerful workflows built using snakemake that simplify the analysis of NGS data. DNA-mapping* ChIP-seq* RNA-seq* ATAC-seq* scRNA-seq Hi-C Whole Genome Bisulfite Seq/WGBS (*Also available in...X. Shirley Liu Lab
The research in our laboratories are focused on the following three areas: Bioinformatics Cancer Epigenetics More at http://liulab.dfci.harvard.edu/
