Neel
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nQuire: A statistical framework for ploidy estimation using NGS short-read data
By Jit 2105 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...The 2014 CeMM PhD Program
For our next PhD Program starting in October 2014 we are looking for exceptionally motivated PhD candidates with a keen interest in genomics and medicine and a strong interest to work in teams. The 2014 CeMM PhD Program will focus on two thematic...ClinCNV: Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data
By Neel 1755 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...JRF @ MANIT
MAULANA AZAD NATIONAL INSTITUTE OF TECHNOLOGY BHOPAL No. CSE/14/1038 Walk in Interview for the post of JRF under TEQIP-II SN Department – Qualification Post Graduation – Time 1 Bio-Informatics & Mathematics M.Tech...LoFreq*: A sequence-quality aware, ultra-sensitive variant caller for NGS data
By BioStar 1722 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...Post doc in Computational Genetics and Genomics at CEINGE Biotecnologie Avanzate, Naples, Italy
We are seeking one motivated scientist to analyze genomics and transcriptomics data of a large collection of neuroblastoma tumors. The successful candidate will be part of a team of researchers with extensive expertise in genome cancer study. He/she...FiNGS: Filters for Next Generation Sequencing
By Neel 1347 days agogithub.com - Key features Filters SNVs from any variant caller to remove false positives Calculates metrics based on BAM files and provides filtering not possible with other tools Fully user-configurable filtering (including which filters to use and their...New version of Modeller, 9.13
By Radha Agarkar 3918 days agoThe new version of Modeller, 9.13, is now available for download!
Libraries or management tools for high throughput sequencing data
Last updated 32 days ago by LEGEGATB Library. The Genome Analysis Toolbox with de-Bruijn graph. A large part of tools developed by the GenScale team are based on this library.These methods enable the analysis of data sets of any size on multi-core desktop...The Best Bioinformatics / Computational Biology Quotes
By Jit 3905 days ago Comments (1)Some funny bioinformatics quotes !!!
