BOL: Related items

nanofilt: Filtering and trimming of long read sequencing data

Jit — Mon, 30 Jul 2018 12:01:52 -0500

Filtering on quality and/or read length, and optional trimming after passing filters.
Reads from stdin, writes to stdout.

Intended to be used:

directly after fastq extraction
prior to mapping
in a stream between extraction and mapping

https://github.com/wdecoster/nanofilt

Address of the bookmark: https://github.com/wdecoster/nanofilt

Project Fellow at IHBT - Palampur, Himachal Pradesh

Sun, 12 Jul 2015 07:54:37 -0500

The Institute is working relentlessly on developing technologies for sustainable utilization of Himalayan bioresources, and in the area of tea, floriculture, bamboos and medicinal and aromatic plants. Looking at the mission of the Institute,the quantum of work undertaken and milestones achieved it was rightly conceived to rename the Institute from CSIR Complex Palampur to Institute of Himalayan Bioresource Technology at a high level meeting. Finally the Institute received its new name Institute of Himalayan Bioresource Technology (IHBT) in 1997 by then Prime Minister Shri H.D. Deve Gowda. Till date this is the only kind of National R&D laboratory in the state of Himachal.

Detail Of Institute of Himalayan Bioresource Technology (IHBT) Project Fellow Recruitment:

No.of Posts: 02

Qualification : 1st Class B. Tech. in Bioinformatics/ Computational Biology Or M.Sc. in Bioinformatics/ Computational Biology with 55% marks OR M.Tech. in Bioinformatics/ Computational Biology with 55% marks.

Age : 28 years as on 10.06.2015

Pay Scale: Rs.12,000/- P.M/Rs.14,000/- P.M.

Age : 35 years,(Up to 40 years for members of SC/STs).

Selection Procedure For Institute of Himalayan Bioresource Technology (IHBT) – Project Fellow Post:

Written Test on 10/06/2015.

Shortlisted candidates will undertake face to face interview.

Dates are yet to be announced for the final selection

Walkin Procedure For Project Fellow vacancy in Institute of Himalayan Bioresource Technology (IHBT):

Eligible candidates may appear for Walk-in-Interview on Date : 10.06.2015, Time 9:00 A.M. Venue : CSIR- IHBT Palampur (H.P.) alongwith an application on prescribed format. Candidates must also bring with them original certificates of testimonials at the time of the appearing for interview failing which he/she will not be allowed to appear for interview.

Important Dates To Remember :
Walk in date for this job : 10/06/2015

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

Assistant Professor/ Professor at Central University of South Bihar

Thu, 16 Jul 2015 22:36:53 -0500

Central University of South Bihar

(Established under Central Universities Act, 2009)

BIT Campus, PO: B.V. College,

Patna – 800 014 (Bihar)

Employment Notice No. CUSB / 27 / Faculty / 2015

Appointment for Faculty Positions Applications in the prescribed form are invited from the eligible candidates for the following posts shown against the subjects to be filled up on regular/contract/re-employment after superannuation basis:

1 Bioinformatics - 03 Posts

2 Biotechnology – 02 Posts

12 Life Science – 04 Posts

The duly filled in application form, complete in all respect along with fee must be sent only by Speed post/Registered post/Courier to The Registrar, Central University of South Bihar, BIT Campus, P.O. : B.V. College, Patna-800014.

Last Date of Receiving Application 10th August, 2015

http://cub.ac.in/index.php?option=com_content&view=article&id=31&Itemid=157

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

JRF in Bioinformatics @ Rajiv Gandhi Centre for Biotechnology (RGCB), Thiruvananthapuram

Sat, 08 Aug 2015 01:22:29 -0500

Rajiv Gandhi Centre for Biotechnology (RGCB), Thiruvananthapuram
Job Code: 060815(10)Y

Jr Research Fellow Posts At Rajiv Gandhi Centre for Biotechnology
Rajiv Gandhi Centre for Biotechnology (RGCB) invites applications to recruit on vacant posts of Junior Research Fellow (JRF). Applications against these Government Jobs can be submitted on or before 15 August 2015.

Rajiv Gandhi Centre for Biotechnology Vacancy 2015 Details
Name of the post – Junior Research Fellow (JRF)
Total vacancies –

Age Limit: Below 28 years as on 15-08-2015.

Qualification(s): Masters Degree in Life Sciences/Biotechnology/Bioinformatics.

How to Apply: Duly filled-in applications in prescribed application format along with copies of required documents should be reach to: Rajiv Gandhi Centre for Biotechnology Thycaud PO, Poojappura, Thiruvananthapuram – 695014, Kerala.

More at http://rgcb.res.in/temporary-position-available-10/

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

Senior Research Fellow (SRF) Bioinformatics at AIIMS, India

Tue, 04 Aug 2015 03:14:32 -0500

DEPARTMENT OF BIOTECHNOLOGY
ALL INDIA INSTITUTE OF MEDICAL SCIENCES
NEW DELHI-110029

Requirement of Senior Research Fellow Applications are invited for the following vacancy under Research project entitled “Exploiting temporal transcription profile, computational analysis and post-transcriptional gene silencing to identify and intercept interactions between host and dormant and actively replicating Mycobacterium tuberculosis”

Senior Research Fellow One

M.Sc. Degree in Biotechnology/ /Microbiology/Bioinformatics and 2 years research experience in the relevant field NET/GATE Qualification with at least 2 years research experience in M. tuberculosis culture and related techniques as well as transcriptome data generation and analysis.

1 year

1. Age relaxation for SC/ST/OBC/PH Candidates will be as per the government rules.

2. Qualification/degree should be from a reputed Institution/University.

3. Mere fulfilling the essential qualification/experience does not guarantee selection.

4. Canvassing in any form will be a disqualification.

5. No TA/DA will be paid either for attending the interview or joining the post.

Interested candidates are to submit their Curriculum Vitae by 5 PM on 17th August, 2015 to Room No.107, Department of Biotechnology, AIIMS, New Delhi-29.

Only shortlisted candidates will be notified by email for interview

www.aiims.edu/images/pdf/recruitment/advertisement/advertisement%20of%20SRF_N1306.pdf

LoFreq*: A sequence-quality aware, ultra-sensitive variant caller for NGS data

BioStar — Tue, 18 Feb 2020 03:24:22 -0600

LoFreq* (i.e. LoFreq version 2) is a fast and sensitive variant-caller for inferring SNVs and indels from next-generation sequencing data. It makes full use of base-call qualities and other sources of errors inherent in sequencing (e.g. mapping or base/indel alignment uncertainty), which are usually ignored by other methods or only used for filtering.

https://github.com/CSB5/lofreq

http://csb5.github.io/lofreq/installation/

https://github.com/CSB5/lofreq/tree/master/dist

Address of the bookmark: http://csb5.github.io/lofreq/

Bioinformatics Symposium

Tue, 11 Aug 2015 04:02:59 -0500

This 2 day symposium will focus on topics in the below mentioned areas.

Experts from India and Japan in this fields will deliver lectures and contribute in discussions. This will provide an opportunity to the participants to interact and learn.

Topics:

Algorithms for biomolecular Sequences / Structures
Bioinformatics databases and tools
High performance computing
Large scale data analysis
Protein function
Structure based drug design
Applications to specific diseases

More at http://www.iitm.ac.in/bioinfo/Symposium-2015/index.html