BOL: Related items

Bioinformatics Faculty at BHARATHIDASAN UNIVERSITY

Sat, 26 Sep 2015 20:34:20 -0500

BHARATHIDASAN UNIVERSITY

(Reaccredited by NAAC with ‘A’ grade)

TIRUCHIRAPPALLI - 620 024

I N V I T E S

APPLICATIONS FOR FACULTY POSITIONS UNDER UGC XII PLAN CREATED POSTS ON CONTRACTUAL BASIS TILL 31.03.2017 IN THE FOLLOWING UNIVERSITY DEPARTMENTS. (Notification No. 31300 /H2/2015, Dt.: 18.09.2015)

ASSISTANT PROFESSOR

1. Bio-Informatics ONE (MBC)

2. Bio-Chemistry ONE G.T.(W)DW

Consolidated Pay of Rs.45,000/- p.m.

Qualification : As per UGC/AICTE/NCTE norms

Application along with other details including specialization can be downloaded from the University website www.bdu.ac.in

LAST DATE FOR RECEIPT OF FILLED IN APPLICATION IS 07.10.2015 BY 5.00 P.M.

More Info : www.bdu.ac.in/adv/UGC_XII_Plan_Contract_Positions.pdf

BASE: a practical de novo assembler for large genomes using long NGS reads

Rahul Nayak — Fri, 19 Oct 2018 07:25:21 -0500

new de novo assembler called BASE. It enhances the classic seed-extension approach by indexing the reads efficiently to generate adaptive seeds that have high probability to appear uniquely in the genome. Such seeds form the basis for BASE to build extension trees and then to use reverse validation to remove the branches based on read coverage and paired-end information, resulting in high-quality consensus sequences of reads sharing the seeds. Such consensus sequences are then extended to contigs.

Address of the bookmark: https://github.com/dhlbh/BASE

R.A Bioinformatics at JNU, Delhi

Tue, 10 May 2016 01:50:38 -0500

R.A Jobs opportunity in Jawaharlal Nehru University (JNU) on purely temporary basis

Project Title : "Structural and functional characterization of serine biosynthetic pathway enzymes from Entamoeba histolytica"

No. of Post : 01

Qualification : Ph.D in any computational biology / bioinformatics

Desirable : 1. Experience with docking, simulations and structural biology with proof of publications is preferred. 2. National Eligibility Test cleared [CSIR/UGC] candidate is preferred.

Salary : According to CSIR rules
How to apply

The application on plain paper indicating name, date of birth/age, address, essential/technical/professional qualifications. experience, list of publications should reach The Prof. S. Gourinath, Principal Investigator, [Project Director], School of Life Sciences, Jawaharlal Nehru University, New Delhi-110067, on or before 23rd May 2016.

More at http://www.jnu.ac.in/Career/currentjobs.htm

nQuire: A statistical framework for ploidy estimation using NGS short-read data

Jit — Thu, 31 Jan 2019 05:12:19 -0600

nQuire implements a set of commands to estimate ploidy level of individuals from species, where recent polyploidization occurred and intraspecific ploidy variation is observed. Specifically, nQuire uses next-generation sequencing data to distinguish between diploids, triploids and tetraploids, on the basis of frequency distributions at variant sites where only two bases are segregating.

For more background see also the publication at BMC Bioinformatics.

https://github.com/clwgg/nQuire

Address of the bookmark: https://github.com/clwgg/nQuire

Research Trainees recruitment in National Agri-Food Biotechnology Institute (NABI)

Sun, 29 Nov 2015 02:47:28 -0600

Research Trainees recruitment in National Agri-Food Biotechnology Institute (NABI)

Eligibility : Pursuing final year of M.Sc./M.Tech.

Subject category for training : I. Agricultural biotechnology II. Computational biology and bioinformatics III. Food Science & Technology IV. Nutrition Science & Technology

Duration of Training : 6 months (January to June 2016)

Selection Procedure : Through screening and selection based on merit, experience, and expression of interest submitted by candidates
How to apply

The last date of application to reach NABI latest by November 30, 2015 by 5:30 PM

More at http://www.nabi.res.in/Training.aspx

ClinCNV: Detection of copy number changes in Germline/Trio/Somatic contexts in NGS data

Neel — Thu, 16 Jan 2020 23:16:02 -0600

ClinCNV detects CNVs in germline and somatic context in NGS data (targeted and whole-genome). We work in cohorts, so it makes sense to try ClinCNV if you have more than 10 samples (recommended amount - 40 since we estimate variances from the data). By "cohort" we mean samples sequenced with the same enrichment kit with approximately the same depth (ie 1x WGS and 30x WGS better be analysed in separate runs of ClinCNV). Of course it is better if your samples were sequenced within the same sequencing facility.

Address of the bookmark: https://github.com/imgag/ClinCNV

M. D. University, Rohtak is looking for the post of Research Associate

Fri, 13 Nov 2015 02:56:48 -0600

M. D. University, Rohtak - Rohtak, Haryana
M. D. University, Rohtak is looking vacancies for the post of Research Associate

Project entitled: "Establish of Bioinformatics Facility for biology teaching through bioinformatics"

Name of post: Research Associate /Trainees

Number of post: 03

Educational Qualification and Experience: Candidates should have Ph D in relevant subjects with experience in handling computational biology resources and software

Selection mode: Walk in interview

How to apply?
Interested and eligible candidates may appear for a walk-in interview on 14th November 2015 at 11.00 am, in the office of Director, Centre for Bioinformatics along with CV and attested copies of all testimonials and additional qualifications.

Recruitment reference: http://www.mdurohtak.ac.in/pdf/career/adv_research_asso_dbt_bioinfo.pdf

Scientist E-II or F in Bioinformatics & Computational Biology at Rajiv Gandhi Centre for Biotechnology

Fri, 13 Nov 2015 03:10:32 -0600

Advt. No.RGCB Advt./SCI 2015/1

Rajiv Gandhi Centre for Biotechnology (RGCB) invites applications for the following three faculty scientist positions:

Scientist G in any of the following disciplines of disease biology: Cancer Research/Cardiovascular Biology/Diabetes Biology/Pathogen Biology
Scientist E-II or F in Bioinformatics & Computational Biology
Scientist E-I or E-II in Cancer Research with special emphasis on Human Papillomavirus Research

More at http://rgcb.res.in/wp-content/uploads/2015/11/APPLICATION-FORMAT-FOR-SCIENTISTS.docx

FiNGS: Filters for Next Generation Sequencing

Neel — Sat, 27 Feb 2021 01:18:35 -0600

Key features

Filters SNVs from any variant caller to remove false positives
Calculates metrics based on BAM files and provides filtering not possible with other tools
Fully user-configurable filtering (including which filters to use and their thresholds)
Option to use filters identical to ICGC recommendations

FiNGS provides researchers with a tool to reproducibly filter somatic variants that is simple to both deploy and use, with filters and thresholds that are fully configurable by the user. It ingests and emits standard variant call format (VCF) files and will slot into existing sequencing pipelines. It allows users to develop and implement their own filtering strategies and simple sharing of these with others.

FiNGS reliably improves upon the precision of default variant caller outputs and performs better than other tools designed for the same task.

Address of the bookmark: https://github.com/cpwardell/FiNGS

Post-doctoral position / Scientist (m/f/d) in Bioinformatics

Mon, 15 Mar 2021 11:34:23 -0500

The Leibniz-Institut für Analytische Wissenschaften - ISAS - e.V. in Dortmund is looking for a Post-doctoral position / Scientist (m/f/d) in Bioinformatics

More at

https://www.isas.de/files/redaktion/jobs/2021/18.60.1_Postdoc_deNBI_06_21_AS.pdf

https://www.isas.de/en/news/062021-post-doctoral-position-scientist-mfd-in-bioinformatics