github.com - Welcome to kevlar, software for predicting de novo genetic variants without mapping reads to a reference genome! kevlar's k-mer abundance based method calls single nucleotide variants (SNVs), multinucleotide variants (MNVs),...
sourceforge.net - Rainbow is developed to provide an ultra-fast and memory-efficient solution to clustering and assembling short reads produced by RAD-seq. First, Rainbow clusters reads using a spaced seed method. Then, Rainbow implements a heterozygote calling like...
Applications are invited for the post of Research Associate (RA) in the ICAR project on "Lactation stress associated postpartum anestrus SNP array in buffaloes". We are looking for a motivated candidate for handling Next Generation sequencing data...
Advertisement No. : R&C/CD/427/2015 ,Vacancy Code: 4271501
Project Fellow Bioinformatics recruitment in Indian Institute of Chemical Biology (IICB) purely temporary
Name of the Project: "Genomics and Informatics Solutions for...
http://last.cbrc.jp/ - LAST can:
Handle big sequence data, e.g:
Compare two vertebrate genomes
Align billions of DNA reads to a genome
Indicate the reliability of each aligned column.
Use sequence quality data properly.
Compare DNA to proteins, with...
Research Scientist/Project Associate/Project Assistant Jobs opportunity in Indian Institute of Technology Madras (IIT Madras)
Research Scientist
Qualification : Ph.D in any branch of life science or bioinformatics or computational biology...
Project Fellow Bioinformatics
Eligibility : MSc(Bio-Chemistry, Bio-Informatics)
Location : Kulu
Last Date : 07 Mar 2016
Hiring Process : Face to Face Interview
Central University of Himachal Pradesh
Project Fellow Bioinformatics Job...
cbio.ensmp.fr - Although centromeres are essential for life and are the subject of extensive research, centromere locations in yeast genomes are difficult to infer, and in most species they are still unknown. Recently, the chromatin conformation assay Hi-C has been...