Jit
Enthusiast computational biologist with business dream !!!
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RNA-seq Analysis Workshop Course Materials
By Jit 2903 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...nanofilt: Filtering and trimming of long read sequencing data
By Jit 2876 days ago Comments (1)github.com - Filtering on quality and/or read length, and optional trimming after passing filters.Reads from stdin, writes to stdout. Intended to be used: directly after fastq extraction prior to mapping in a stream between extraction and...nQuire: a statistical framework for ploidy estimation using next generation sequencing
By Jit 2810 days agogithub.com - nQuire provides a statistical framework to study organisms with intraspecific variation in ploidy. nQuire is likely to be useful in epidemiological studies of pathogens, artificial selection experiments, and for historical or ancient samples where...IPython: Interactive notebooks
By Rahul Nayak 4237 days agoThe IPython Notebook is a web-based interactive computational environment where you can combine code execution, text, mathematics, plots and rich media into a single documentAMStat: display statistics of large sequence files from next generation sequencing projects
By Neel 2774 days agosamstat.sourceforge.net - SAMStat is an efficient C program to quickly display statistics of large sequence files from next generation sequencing projects. When applied to SAM/BAM files all statistics are reported for unmapped, poorly and accurately mapped reads...snakepipes: A toolkit based on snakemake and python for analysis of NGS data
By Jit 2572 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...NIAB Molecular Biology/Bioinformatics Scientist/RA Openings
D. No. 1-121/1, 4th and 5th Floors, Axis Clinicals Building, Miyapur, Hyderabad, Telangana, India- 500 049 Email: admin@niab.org.in Telephones: +91 40 2304 9403 Telefax: +91 40 2304 2740 Advertisement No: 5/2014 About NIAB National Institute...ClinCNV: Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data
By Neel 2340 days agogithub.com - ClinCNV detects CNVs in germline and somatic context in NGS data (targeted and whole-genome). We work in cohorts, so it makes sense to try ClinCNV if you have more than 10 samples (recommended amount - 40 since we estimate variances from...Bioinformatics JRF/RA/SRF position at PANJAB UNIVERSITY
CENTRE FOR SYSTEMS BIOLOGY & BIOINFORMATICS UIEAST, PANJAB UNIVERSITY, CHANDIGARH Applications are invited along with complete bio-data and attested copies of certificates of qualifications, experience etc. for the one post of Research...LoFreq*: A sequence-quality aware, ultra-sensitive variant caller for NGS data
By BioStar 2308 days agocsb5.github.io - LoFreq* (i.e. LoFreq version 2) is a fast and sensitive variant-caller for inferring SNVs and indels from next-generation sequencing data. It makes full use of base-call qualities and other sources of errors inherent in sequencing (e.g. mapping or...
