<![CDATA[BOL: Related items]]> https://bioinformaticsonline.com/related/36880?offset=630 https://bioinformaticsonline.com/bookmarks/view/38892/wtdbg2-a-fuzzy-bruijn-graph-approach-to-long-noisy-reads-assembly Mon, 04 Feb 2019 04:53:47 -0600 https://bioinformaticsonline.com/bookmarks/view/38892/wtdbg2-a-fuzzy-bruijn-graph-approach-to-long-noisy-reads-assembly <![CDATA[wtdbg2: A fuzzy Bruijn graph approach to long noisy reads assembly]]> Wtdbg2 is a de novo sequence assembler for long noisy reads produced by PacBio or Oxford Nanopore Technologies (ONT). It assembles raw reads without error correction and then builds the consensus from intermediate assembly output. 

./wtdbg2 -x rs -g 4.6m -t 16 -i reads.fa.gz -fo prefix
./wtpoa-cns -t 16 -i prefix.ctg.lay.gz -fo prefix.ctg.fa

Address of the bookmark: https://github.com/ruanjue/wtdbg2

]]> BioStar https://bioinformaticsonline.com/opportunity/view/25306/research-trainees-recruitment-in-national-agri-food-biotechnology-institute-nabi Sun, 29 Nov 2015 02:47:28 -0600 <![CDATA[Research Trainees recruitment in National Agri-Food Biotechnology Institute (NABI)]]> 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

]]> https://bioinformaticsonline.com/bookmarks/view/40701/fastgt-an-alignment-free-method-for-calling-common-snvs-directly-from-raw-sequencing-reads Tue, 28 Jan 2020 03:27:33 -0600 https://bioinformaticsonline.com/bookmarks/view/40701/fastgt-an-alignment-free-method-for-calling-common-snvs-directly-from-raw-sequencing-reads <![CDATA[FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads]]> FastGT is a program package for whole-genome genotyping of genome variants directly from raw sequencing reads. It is written in C and runs in Linux. FastGT uses a list of variant-specific k-mer pairs that are unique in human genome, counts the frequency of k-mers in sequencing data and predicts the genotype. All this takes less than 1 hour on average low-cost Linux server.

http://bioinfo.ut.ee/FastGT/

https://github.com/bioinfo-ut/GenomeTester4/

Address of the bookmark: http://bioinfo.ut.ee/FastGT/

]]> Jit https://bioinformaticsonline.com/opportunity/view/25251/m-d-university-rohtak-is-looking-for-the-post-of-research-associate Fri, 13 Nov 2015 02:56:48 -0600 <![CDATA[M. D. University, Rohtak is looking for the post of Research Associate]]> 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

]]> https://bioinformaticsonline.com/bookmarks/view/41030/slr-superscaffolder-a-scaffold-assemble-pipeline-for-stlfr-reads Fri, 14 Feb 2020 14:23:30 -0600 https://bioinformaticsonline.com/bookmarks/view/41030/slr-superscaffolder-a-scaffold-assemble-pipeline-for-stlfr-reads <![CDATA[SLR-superscaffolder: A scaffold assemble pipeline for stLFR reads.]]> This is a scaffold assembler designed for stLFR reads[1]. It uses the link-reads information from stLFR reads to assemble contigs to scaffolds.

Here is an illustration of this pipeline:

 image

Address of the bookmark: https://github.com/BGI-Qingdao/SLR-superscaffolder

]]> Jit https://bioinformaticsonline.com/opportunity/view/25253/scientist-e-ii-or-f-in-bioinformatics-computational-biology-at-rajiv-gandhi-centre-for-biotechnology Fri, 13 Nov 2015 03:10:32 -0600 <![CDATA[Scientist E-II or F in Bioinformatics & Computational Biology at Rajiv Gandhi Centre for Biotechnology]]> 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

]]> https://bioinformaticsonline.com/bookmarks/view/42132/squeezemeta-a-fully-automated-metagenomics-pipeline-from-reads-to-bins Mon, 17 Aug 2020 05:25:10 -0500 https://bioinformaticsonline.com/bookmarks/view/42132/squeezemeta-a-fully-automated-metagenomics-pipeline-from-reads-to-bins <![CDATA[SqueezeMeta: a fully automated metagenomics pipeline, from reads to bins]]> SqueezeMeta is a full automatic pipeline for metagenomics/metatranscriptomics, covering all steps of the analysis. SqueezeMeta includes multi-metagenome support allowing the co-assembly of related metagenomes and the retrieval of individual genomes via binning procedures. Thus, SqueezeMeta features several unique characteristics:

  1. Co-assembly procedure with read mapping for estimation of the abundances of genes in each metagenome
  2. Co-assembly of a large number of metagenomes via merging of individual metagenomes
  3. Includes binning and bin checking, for retrieving individual genomes
  4. The results are stored in a database, where they can be easily exported and shared, and can be inspected anywhere using a web interface.
  5. Internal checks for the assembly and binning steps inform about the consistency of contigs and bins, allowing to spot potential chimeras.
  6. Metatranscriptomic support via mapping of cDNA reads against reference metagenomes

Address of the bookmark: https://github.com/jtamames/SqueezeMeta

]]> BioStar https://bioinformaticsonline.com/opportunity/view/42955/post-doctoral-position-scientist-mfd-in-bioinformatics Mon, 15 Mar 2021 11:34:23 -0500 <![CDATA[Post-doctoral position / Scientist (m/f/d) in Bioinformatics]]> 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

]]> https://bioinformaticsonline.com/bookmarks/view/42946/aligngraph2-similar-genome-assisted-reassembly-pipeline-for-pacbio-long-reads Sun, 14 Mar 2021 09:42:47 -0500 https://bioinformaticsonline.com/bookmarks/view/42946/aligngraph2-similar-genome-assisted-reassembly-pipeline-for-pacbio-long-reads <![CDATA[AlignGraph2: similar genome-assisted reassembly pipeline for PacBio long reads]]> AlignGraph2 is the second version of AlignGraph for PacBio long reads. It extends and refines contigs assembled from the long reads with a published genome similar to the sequencing genome.

More at https://academic.oup.com/bib/advance-article-abstract/doi/10.1093/bib/bbab022/6146772

Address of the bookmark: https://github.com/huangs001/AlignGraph2

]]> Rahul Nayak https://bioinformaticsonline.com/opportunity/view/25287/postdoc-position-in-bioinformatics-irccs-milan-italy Wed, 25 Nov 2015 03:38:38 -0600 <![CDATA[PostDoc position in Bioinformatics - IRCCS - Milan - Italy]]> PostDoc position in Bioinformatics

A full-time post-doctoral position for a bioinformatician with experience in managing and analyzing NGS data is available in the Laboratory of Molecular Cardiology at Policlinico San Donato-IRCCS, Milan, Italy. For lab publications, see: http://scholar.google.it/citations?user=wAPKO9wAAAAJ&hl=it&oi=ao

https://www.researchgate.net/profile/Fabio_Martelli

The goal of the project is investigating the regulation and functional role of non coding RNAs in tissue response to hypoxia and ischemia.

We are looking for a candidate that is going to interact with biologists and bioinformaticians to manage and analyze NGS data (mostly RNA-seq) and microarray data.

The successful candidate must have a minimum of 3 years experience in dealing with NGS data, a good command of English and written communication and at least 2 relevant publications as first author in peer reviewed international journals. The candidate is expected to interact with a small international group and to be able also to work independently. Knowledge of programming is a definitive plus, as well as a good statistical background and/or wet molecular biology skills.

Salary is proportional to experience and to the publication record (up to 38 000euro/year before taxes and retirement contribution i.e. IRPEF and INPS).

Please, send your CV by e-mail to Fabio Martelli:

fabio.martelli@grupposandonato.it

Location: Laboratory of Molecular Cardiology at Policlinico San Donato-IRCCS, Milan, Italy.
Link: https://www.researchgate.net/profile/Fabio_Martelli
Contact person: Fabio Martelli
Contact email: fabio.martelli@grupposandonato.it

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