BOL: Related items

One-Year Internship In Computational Biology & Bioinformatics

Mon, 04 Apr 2016 05:35:57 -0500

This one-year internship program has an inter-disciplinary curriculum that rests on research strengths and infrastructure at the computational biology & bioinformatics facility at Rajiv Gandhi Centre for Biotechnology . Using live demonstration platforms of high end genomic analysis systems including next generation sequencing, advanced proteomics platforms, advanced bio-imaging, student seminars in addition to computer laboratory based courses, interns will get state of the art exposure and training in application of bioinformatics to biomedical research.The internship involves 8 months of hands on training in wet and dry laboratory methods and a four-month dissertation. This internship program is designed for students who would like to gain good knowledge and experience in Bioinformatics as a prelude to taking up a PhD course or look for employment opportunities. The subjects covered during the internship will include but not limited to:
• Systems Biology
• Genomic Informatics
• Proteomic Informatics
• Biomedical Text Mining
• Ontologies
• Data Integration
• Data Mining
• Protein Structure & Function
• Metabolomics
• Molecular Evolution
• Pathways & Networks
• Resource Development
• Scripting & Algorithms
Qualifications: Admission to the Internship requires a first class degree in Engineering Sciences (Biotechnology/Computer Science), Medical/Dental/Pharmaceutical Sciences (MBBS or BDS or BAM or B.Pharm) or a Masters degree in Life Science, Medical Laboratory Technology, Biotechnology, Bioinformatics or Computer Science.
Internship Fees: The internship fee for the 12-month program is Rupees 70,000 (Rupees Seventy thousand). This is payable as an initial admission fee of Rs. 10,000 followed by payments of Rs. 6,000 monthly from months 3 to 9. The final completion certificate will be given after payment of all fees.
Mode of Selection: Selection will be based on interview and the top 5 candidates will be shortlisted for the program.
Location: Thiruvananthapuram

More at http://rgcb.res.in/TrainingPrograms/internship.php

Sequence assembly with MIRA 4

Priya Singh — Wed, 06 Apr 2016 08:21:22 -0500

MIRA is a multi-pass DNA sequence data assembler/mapper for whole genome and EST/RNASeq projects. MIRA assembles/maps reads gained by

electrophoresis sequencing (aka Sanger sequencing)
454 pyro-sequencing (GS20, FLX or Titanium)
Ion Torrent
Solexa (Illumina) sequencing
(in development) Pacific Biosciences sequencing

into contiguous sequences (called contigs). One can use the sequences of different sequencing technologies either in a single assembly run (a true hybrid assembly) or by mapping one type of data to an assembly of other sequencing type (a semi-hybrid assembly (or mapping)) or by mapping a data against consensus sequences of other assemblies (a simple mapping).

The MIRA acronym stands for Mimicking Intelligent Read Assembly and the program pretty well does what its acronym says (well, most of the time anyway). It is the Swiss army knife of sequence assembly that I've used and developed during the past 14 years to get assembly jobs I work on done efficiently - and especially accurately. That is, without me actually putting too much manual work into it.

More at http://mira-assembler.sourceforge.net/docs/DefinitiveGuideToMIRA.html

Address of the bookmark: http://mira-assembler.sourceforge.net/docs/DefinitiveGuideToMIRA.html

Understanding Fastqc Output

Jit — Fri, 15 Apr 2016 05:47:40 -0500

Understanding Following table and graphs

Duplication level
kmer profile
per base GC content
per base N content
per base quality
per base sequence content
per sequence GC content
per sequence quality
sequence length distribution

More at http://www.bioinformatics.babraham.ac.uk/projects/fastqc/Help/3%20Analysis%20Modules/

Address of the bookmark: http://www.bioinformatics.babraham.ac.uk/projects/fastqc/Help/3%20Analysis%20Modules/

ALE: a Generic Assembly Likelihood Evaluation Framework for Assessing the Accuracy of Genome and Metagenome Assemblies

Neel — Tue, 26 Apr 2016 03:38:43 -0500

Assembly Likelihood Evaluation (ALE) framework that overcomes these limitations, systematically evaluating the accuracy of an assembly in a reference-independent manner using rigorous statistical methods. This framework is comprehensive, and integrates read quality, mate pair orientation and insert length (for paired-end reads), sequencing coverage, read alignment and k-mer frequency. ALE pinpoints synthetic errors in both single and metagenomic assemblies, including single-base errors, insertions/deletions, genome rearrangements and chimeric assemblies presented in metagenomes. At the genome level with real-world data, ALE identifies three large misassemblies from the Spirochaeta smaragdinae finished genome, which were all independently validated by Pacific Biosciences sequencing. At the single-base level with Illumina data, ALE recovers 215 of 222 (97%) single nucleotide variants in a training set from a GC-rich Rhodobacter sphaeroides genome. Using real Pacific Biosciences data, ALE identifies 12 of 12 synthetic errors in a Lambda Phage genome, surpassing even Pacific Biosciences' own variant caller, EviCons. In summary, the ALE framework provides a comprehensive, reference-independent and statistically rigorous measure of single genome and metagenome assembly accuracy, which can be used to identify misassemblies or to optimize the assembly process.

More at http://www.ncbi.nlm.nih.gov/pubmed/23303509

Address of the bookmark: http://sc932.github.io/ALE/about.html

MEDEA: Comparative Genomic Visualization with Adobe Flash

Jit — Tue, 26 Apr 2016 12:15:16 -0500

As the number of sequence and annotated genomes grows larger, the need to understand, compare, and contrast the data becomes increasingly important. Using the power of the human visual system to detect trends and spot outliers is necessary in such large and complex data sets.

More at http://www.broadinstitute.org/annotation/medea/

Address of the bookmark: http://www.broadinstitute.org/annotation/medea/

RASTtk : algorithm for building custom annotation pipelines and annotating batches of genomes

Abhi — Wed, 27 Apr 2016 11:07:59 -0500

The RAST (Rapid Annotation using Subsystem Technology) annotation engine was built in 2008 to annotate bacterial and archaeal genomes. It works by offering a standard software pipeline for identifying genomic features (i.e., protein-encoding genes and RNA) and annotating their functions. Recently, in order to make RAST a more useful research tool and to keep pace with advancements in bioinformatics, it has become desirable to build a version of RAST that is both customizable and extensible. In this paper, we describe the RAST tool kit (RASTtk), a modular version of RAST that enables researchers to build custom annotation pipelines. RASTtk offers a choice of software for identifying and annotating genomic features as well as the ability to add custom features to an annotation job. RASTtk also accommodates the batch submission of genomes and the ability to customize annotation protocols for batch submissions. This is the first major software restructuring of RAST since its inception.

More at http://www.nature.com/articles/srep08365

Address of the bookmark: http://rast.nmpdr.org/

Bioinformatics National Certification (BINC) Examination 2016

Wed, 11 May 2016 02:17:44 -0500

Bioinformatics National Certification (BINC) Examination 2016

Department of Biotechnology, Government of India, New Delhi & Pondicherry University, Puducherry

Starting of online submission of application : April 13, 2016

Last date for submission of application : May 13, 2016

Examination consists of two parts:

Part - I (Paper - I) : June 12, 2016 (10 AM -12 PM)
Part - II (Paper • II & III) : June 26, 2016 (9 AM • 12 PM & 2 PM • 4 PM)

Objective: Pondicherry University, on behalf of the Department of Biotechnology (DBT),
Government of India, will conduct the Bioinformatics National Certification (BING) examination. The objective of this examination is to identify Bioinformatics professionals
for further studies as well as to help potential employers in recruitment of candidates having exceptionally good Bioinformatics skills.

Eligibility : Bachelor degree in Life Sciences, Physical Sciences, Chemical Sciences, Mathematical Sciences, Agriculture, Veterinary, Medicine, Pharmacy, Engineering and Technology are eligible to appear for the examination. They need not have any formal training, diploma or certificate in Bioinformatics.

Application and syllabus : The online application can be filled from April 13, 2016 to May 13, 2016.

Syllabus for the examination is available online.

It consists of five sections:
Bioinformatics, Biology, Physical and Chemical Sciences, Mathematics & Statistics and Computer Science & Information Technology.

Examination : The examination fee is Rs. 600/- for general candidates, Rs. 400/- for women/OBC candidates and Rs. 200 for SC/ST candidates, and no fee for physically challenged candidates.

The online Part - I (Paper - I) examination is scheduled on June 12,2016 and Part- II (Paper - II and Paper- III) on June 26, 2016. The Paper- I will be of objective type and candidates scoring a minimum of 40% marks in Paper - I will be called to appear in Part II examination.

Part II examination consists of two papers : The Paper - II will be of short answer type questions of three hours duration while the Paper- III will be a practical examination of two hours duration to test analytical ability and programming skill of candidates.

Research Fellowships for all the successful candidates those who are interested and qualified in pursuing Ph.D. in India will be awarded. In addition, cash prizes will be awarded to the top 10 successful candidates.

The details of examination centres, other details and submission of application, please
visit: http://www.pondiuni.edu.in/exams/binc/

BINC 2016

Jit — Wed, 11 May 2016 07:15:03 -0500

Bioinformatics National Certification (BINC) Examination 2016

Department of Biotechnology, Government of India, New Delhi & Pondicherry University, Puducherry

Starting of online submission of application : April 13, 2016

Last date for submission of application : May 13, 2016

Examination consists of two parts:

Part - I (Paper - I) : June 12, 2016 (10 AM -12 PM)
Part - II (Paper • II & III) : June 26, 2016 (9 AM • 12 PM & 2 PM • 4 PM)

Application and syllabus : The online application can be filled from April 13, 2016 to May 13, 2016.

Syllabus for the examination is available online.

It consists of five sections:
Bioinformatics, Biology, Physical and Chemical Sciences, Mathematics & Statistics and Computer Science & Information Technology.

Examination : The examination fee is Rs. 600/- for general candidates, Rs. 400/- for women/OBC candidates and Rs. 200 for SC/ST candidates, and no fee for physically challenged candidates.

The details of examination centres, other details and submission of application, please
visit: http://www.pondiuni.edu.in/exams/binc/

Do you think it's important for everyone to pass BINC exam?

Jit — Wed, 11 May 2016 07:25:34 -0500

The Department of Biotechnology (DBT), Government of India has instituted BINC examination with the objective of evaluating the Bioinformatics knowledge & skills of students. Do you think it is important ?

Sample BINC question paper 2016 - part1

Radha Agarkar — Fri, 13 May 2016 03:41:48 -0500

Please download the sample bioinformatics question paper for BINC 2016