Rahul Agarwal
I'm a Bioinformatician and Programmer
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ChopStitch: exon annotation and splice graph construction using transcriptome assembly and whole...
By Rahul Nayak 2337 days agogithub.com - ChopStitch is a new method for finding putative exons and constructing splice graphs using an assembled transcriptome and whole genome shotgun sequencing (WGSS) data. ChopStitch identifies exon-exon boundaries in de novo assembled RNA-seq data with...Post-Doc Positions at the Institute of Evolution, University of Haifa, Haifa, Israel
We are looking for independent, motivated, diligent, laborious, dedicated Bioinformaticians as post-doctorate fellows for a project aimed at revealing the mechanisms of cancer-resistance and anti-cancer activity of the hypoxia-tolerant subterranean,...PureCN: copy number calling and SNV classification using targeted short read sequencing
By Jit 2300 days agobioconductor.org - This package estimates tumor purity, copy number, and loss of heterozygosity (LOH), and classifies single nucleotide variants (SNVs) by somatic status and clonality. PureCN is designed for targeted short read sequencing data, integrates well with...Software engineer/Computational Biologist - Equinome Ltd., Dublin, Ireland
Equinome (www.equinome.com) is the world leader in the research and development of state-of-the-art novel genomic tools to inform the breeding, selection and training of Thoroughbred racehorses. Since its launch in 2010, Equinome has successfully...LoRMA: A tool for correcting sequencing errors in long reads
By Abhimanyu Singh 2272 days agogite.lirmm.fr - An error correction method that uses long reads only. The method consists of two phases: first, we use an iterative alignment-free correction method based on de Bruijn graphs with increasing length of k-mers, and second, the corrected reads are...Project Assistant Position at JMI
Project Assistant Position (@ Rs.10,000/pm Fixed) is available for one year ina research project funded by the Department of Science and Technology entitled, "Folding and stability of naturally truncated photosynthetic pigment,C- phycoerythrin from...VariantBam: Filtering and profiling of next-generational sequencing data using region-specific rules
By Rahul Nayak 2244 days agogithub.com - VariantBam is a tool to extract/count specific sets of sequencing reads from next-generational sequencing files. To save money, disk space and I/O, one may not want to store an entire BAM on disk. In many cases, it would be more efficient to store...JAMIA HAMDARD Bioinformatics Faculty Jobs 2014
JAMIA HAMDARD (Deemed University) Hamdard Nagar, New Delhi – 110 062 R E C R U I T M E N T (Advertisement No. 5/2014) Applications on prescribed form are invited for filling up the following teaching positions in the Department of...NanoPack: visualizing and processing long-read sequencing data
By Jit 2161 days agogithub.com - The NanoPack tools are written in Python3 and released under the GNU GPL3.0 License. The source code can be found at https://github.com/wdecoster/nanopack, together with links to separate scripts and their documentation. The scripts are compatible...Joao Pedro de Magalhaes Lab
Ageing has a profound impact on human society and modern medicine, yet it remains a major puzzle of biology. The goal of my work is to help understand the genetic, cellular, and molecular mechanisms of ageing. In the long term, I would like my work...
