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Walk in for Research Asst & Programmer Enterovirus Research Centre Mumbai - India
Enterovirus Research Centre Mumbai Jobs 2015 – Walk in for Research Asst & Programmer Posts: Enterovirus Research Centre, Mumbai, Indian Council of Medical Research has issued notification for the recruitment of Research Asst & Programmer...nanofilt: Filtering and trimming of long read sequencing data
By Jit 2310 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...
BINC Sample Question Paper !!!
By Jitendra Narayan 3511 days agoBINC sample question paper round THREE ...BASE: a practical de novo assembler for large genomes using long NGS reads
By Rahul Nayak 2229 days agogithub.com - new de novo assembler called BASE. It enhances the classic seed-extension approach by indexing the reads efficiently to generate adaptive seeds that have high probability to appear uniquely in the genome. Such seeds form the basis for BASE...Senior Research Fellow (SRF) Bioinformatics at Central Institute for Research on Buffaloes
Senior Research Fellow (SRF) Bioinformatics at Central Institute for Research on Buffaloes Address: Central Institute for Research on Buffaloes, Sirsa Road, Hisar State: Haryana Pay Scale: Post Graduate in subjects other than Veterinary Science...nQuire: A statistical framework for ploidy estimation using NGS short-read data
By Jit 2125 days agogithub.com - nQuire implements a set of commands to estimate ploidy level of individuals from species, where recent polyploidization occurred and intraspecific ploidy variation is observed. Specifically, nQuire uses next-generation sequencing data to distinguish...Savitribai Phule Pune University Recruitment for 04 JRF Post in April 2015
Savitribai Phule Pune University announced application for recruitment to the post of Junior Research Fellow. The candidates for the post can apply through prescribed format before 10 May 2015. Description: Important Date &...ClinCNV: Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data
By Neel 1774 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...LoFreq*: A sequence-quality aware, ultra-sensitive variant caller for NGS data
By BioStar 1742 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...
