Jit
Enthusiast computational biologist with business dream !!!
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Rosenberg lab
Research. Research in the lab focuses on mathematical, statistical, and computational problems in evolutionary biology and human genetics. Long-term interests of the lab include topics such as: Human genetic variation Inference of human...Understanding HiFi Reads !
By Rahul Nayak 977 days agopacb.com - While little public data is available for either of the new synthetic long read approaches, Illumina showed an example comparison earlier this year at the Festival of Genomics & Biodata conference (FoG 2022). In the IGV screenshot...JRF Bioinformatics @ ICAR - National Research Centre for Orchids Pakyong
ICAR - National Research Centre for Orchids Pakyong F.No:NRCO/Admn/DBT /136 / Walk-in-Interviews will be held at 737106, Sikkim for the post of 01 (One Project ‘DBT’s Twinning programme for the NE’ titled “Assessment of some fragrant...1mb long DNA with Nanopore technology
By Jit 2533 days agoLongest read of 1mb achievements with Nanopore
Frequent words problem solution by Perl
Last updated 3457 days ago by JitSolved with perl http://rosalind.info/problems/1a/ #Find the most frequent k-mers in a string.#Given: A DNA string Text and an integer k.#Return: All most frequent k-mers in Text (in any order).use strict;use warnings;my...NanoPack: visualizing and processing long-read sequencing data
By Jit 2162 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...-
Clump Finding Problem Solved with Perl
Last updated 2538 days ago by JitThe question at http://rosalind.info/problems/1d/ Script are moved to http://bioinformaticsonline.com/snippets/view/34633/clump-finding-problem-solved-with-perl Kevler: Reference-free variant discovery in large eukaryotic genomes
By Jit 1763 days agogithub.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),...SVEngine: Allele Specific and Haplotype Aware Structural Variants Simulator
By Jit 1605 days ago Comments (1)bitbucket.org - SVEngine (Structural Variants Engine) SVEngine is a multi-purpose and self-contained simulator for whole genome scale spike-in of thousands of SV events of various types in both single-sample and matched sample scenarios. SVEngine takes as input...RA at University of Delhi
Research Scientist Jobs opportunity in University of Delhi on temporary basis Qualifications : Ph. D. Desirable : Experience on DNA Markers, plant genome mapping and bioinformatics No. of Post : 03 Department : Genetics Salary : Rs....
