Radha Agarkar
A Bioinformatician
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BINC Sample Question Paper !!!
By Jitendra Narayan 4192 days agoBINC sample question paper round THREE ...Magic-BLAST: a tool for mapping large next-generation RNA or DNA sequencing runs against a whole...
By Jit 3206 days agoncbi.github.io - Magic-BLAST is a tool for mapping large next-generation RNA or DNA sequencing runs against a whole genome or transcriptome. Each alignment optimizes a composite score, taking into account simultaneously the two reads of a pair, and in case of...Senior Research Fellow (SRF) Bioinformatics at Central Institute for Research on Buffaloes
Senior Research Fellow (SRF) Bioinformatics at Central Institute for Research on Buffaloes Address: Central Institute for Research on Buffaloes, Sirsa Road, Hisar State: Haryana Pay Scale: Post Graduate in subjects other than Veterinary Science...HapCUT2: robust and accurate haplotype assembly for diverse sequencing technologies
By Jit 3067 days agogithub.com - HapCUT2 is a maximum-likelihood-based tool for assembling haplotypes from DNA sequence reads, designed to "just work" with excellent speed and accuracy. We found that previously described haplotype assembly methods are specialized for specific read...Savitribai Phule Pune University Recruitment for 04 JRF Post in April 2015
Savitribai Phule Pune University announced application for recruitment to the post of Junior Research Fellow. The candidates for the post can apply through prescribed format before 10 May 2015. Description: Important Date &...gSearch: a fast and flexible general search tool for whole-genome sequencing
By Jit 2983 days agoml.ssu.ac.kr - gSearch compares sequence variants in the Genome Variation Format (GVF) or Variant Call Format (VCF) with a pre-compiled annotation or with variants in other genomes. Its search algorithms are subsequently optimized and implemented in a...Indexcov: fast coverage quality control for whole-genome sequencing
By Jit 2961 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...Appointment of two traineeships and two studentships in Bioinformatics
Applications are invited for the appointment of two traineeships and two studentships in Bioinformatics for a period of six months sponsored by Department of Biotechnology, Government of India in the Bioinformatics Sub-DIC, Saraswathy Thangavelu...EXCAVATOR: detecting copy number variants from whole-exome sequencing data
By Radha Agarkar 2832 days agosourceforge.net - EXCAVATOR, for the detection of copy number variants (CNVs) from whole-exome sequencing data. EXCAVATOR combines a three-step normalization procedure with a novel heterogeneous hidden Markov model algorithm and a calling method that classifies...Narcis Fernandez-Fuentes Lab
Welcome to our web-site compiling all the research-related activities of the group. Our research interests relate to a number of areas within Bioinformatics. We have a long-standing interest in protein structure prediction and structure-to-function...
