Rahul Nayak
A Bioinformatician
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NextSV: a meta-caller for structural variants from low-coverage long-read sequencing data
By Jit 2302 days agogithub.com - NextSV, a meta SV caller and a computational pipeline to perform SV calling from low coverage long-read sequencing data. NextSV integrates three aligners and three SV callers and generates two integrated call sets (sensitive/stringent) for different...Indexcov: fast coverage quality control for whole-genome sequencing
By Jit 2279 days ago Comments (1)github.com - indexcov, an efficient estimator of whole-genome sequencing coverage to rapidly identify samples with aberrant coverage profiles, reveal large-scale chromosomal anomalies, recognize potential batch effects, and infer the sex of a...lordFAST: sensitive and Fast Alignment Search Tool for LOng noisy Read sequencing Data
By BioJoker 2190 days agogithub.com - lordFAST is a sensitive tool for mapping long reads with high error rates. lordFAST is specially designed for aligning reads from PacBio sequencing technology but provides the user the ability to change alignment parameters depending on the reads...Flye: Fast and accurate de novo assembler for single molecule sequencing reads
By Rahul Nayak 1969 days agogithub.com - Flye is a de novo assembler for single molecule sequencing reads, such as those produced by PacBio and Oxford Nanopore Technologies. It is designed for a wide range of datasets, from small bacterial projects to large mammalian-scale assemblies. The...Kamaleshwar Singh Lab
The focus of Dr. Singh’s research and teaching is on the molecular mechanistic basis for environmental carcinogen-induced genetic (DNA damage) and epigenetic changes, and susceptibility to human cancer development More at...FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads
By Jit 1763 days agobioinfo.ut.ee - FastGT is a program package for whole-genome genotyping of genome variants directly from raw sequencing reads. It is written in C and runs in Linux. FastGT uses a list of variant-specific k-mer pairs that are unique in human genome, counts the...FastProNGS: fast preprocessing of next-generation sequencing reads
By Rahul Nayak 1429 days agogithub.com - FastProNGS to integrate the quality control process with automatic adapter removal. Parallel processing was implemented to speed up the process by allocating multiple threads. Compared with similar up-to-date preprocessing tools, FastProNGS is by...Bioinformatics Centre, Bose Institute vacancy of Research Associate / Senior Research Fellow
Bioinformatics Centre, Bose Institute vacancy of Research Associate / Senior Research Fellow Location where with post of Research Associate / Senior Research Fellow is available: Bioinformatics Centre, Bose Institute in Kolkata, West...Bioinformatics Trainee at University of Kalyani
Bioinformatics Trainee Eligibility : MSc Location : Kolkata Last Date : 28 Dec 2015 Hiring Process : Walk - In University of Kalyani Bioinformatics Trainee Job position in University of Kalyani Number of Posts : 02 Qualification : M.Sc....Chekulaevalab
Focusing on understanding the molecular mechanisms that regulate mRNA translation, localization and stability and role of non-coding RNAs in this process. Up to 90% of human DNA is estimated to be transcribed into so called non-coding RNAs that are...
