Jit
Enthusiast computational biologist with business dream !!!
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JRF Bioinformatics at National Chemical Laboratory
Junior Project Fellow Bioinformatics Eligibility : ME/M.Tech, MSc(Bio-Informatics) Location : Pune Last Date : 08 Jan 2016 Hiring Process : Written-test, Face to Face Interview National Chemical Laboratory Junior Project Fellow Jobs...Bioinformatics tools for telomere to telomere assembly !
By BioStar 1762 days agooptimize HiFi readsJRF Bioinformatics at CUK
JRF Bioinformatics Eligibility : MSc(Bio-Informatics), BE/B.Tech Location : Kasaragod Last Date : 20 Dec 2015 Hiring Process : Face to Face Interview Central University of Kerala JRF job opportunity in Central University of Kerala...QuorUM: An Error Corrector for Illumina Reads
By Jit 3140 days agojournals.plos.org - Illumina Sequencing data can provide high coverage of a genome by relatively short (most often 100 bp to 150 bp) reads at a low cost. Even with low (advertised 1%) error rate, 100 × coverage Illumina data on average has an error in some read...JRF/Traineeship/Studentship Bioinformatics
JRF/Traineeship/Studentship Bioinformatics Eligibility : ME/M.Tech(Bio-Informatics/Bio-Chemistry Engg, CSE), MSc(Bio-Informatics, CS) Location : Delhi Last Date : 18 Dec 2015 Hiring Process : Walk - In IARI - Job...QuorUM: An Error Corrector for Illumina Reads
By BioStar 2322 days agowww.genome.umd.edu - We produce trimmed and error-corrected reads that result in assemblies with longer contigs and fewer errors. We compared QuorUM against several published error correctors and found that it is the best performer in most metrics we use. QuorUM is...JRF Bioinformatics job position in University of Hyderabad
JRF Bioinformatics Eligibility : ME/M.Tech(Bio-Informatics/Bio-Chemistry Engg), MSc(Bio-Informatics) Location : Hyderabad Last Date : 30 Dec 2015 Hiring Process : Written-test University of Hyderabad JRF Bioinformatics job position...JASMINE: Jointly Accurate Sv Merging with Intersample Network Edges
By Shruti Paniwala 1443 days agogithub.com - This tool is used to merge structural variants (SVs) across samples. Each sample has a number of SV calls, consisting of position information (chromosome, start, end, length), type and strand information, and a number of other values. Jasmine...Hoffman Lab
They develop machine learning techniques to better understand chromatin biology. These models and algorithms transform high-dimensional functional genomics data into interpretable patterns and lead to new biological...VG: variation graph data structures, interchange formats, alignment, genotyping, and variant...
By Jit 2330 days agogithub.com - Variation graphs provide a succinct encoding of the sequences of many genomes. A variation graph (in particular as implemented in vg) is composed of: nodes, which are labeled by sequences and ids edges, which connect two nodes via either of...
