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Choosing the Right NGS Sequencing Instrument for Your Study
By Neel 1460 days agogenohub.com - The right sequencing instrument for your study depends on your project goal. Setting aside turnaround time and price, it essentially comes down to the numbers of reads and read length you need for your experiment. Below, we've described and compared...RA Bioinformatics at NIPGR
Applications are invited from suitable candidates for filling up one position of Research Associate (RA) in the Institute with Dr. Senthil-Kumar Muthappa, Scientist, NIPGR, in the scheme of "Short-Term Research Fellowship" programme. The position is...Common steps for reads mapping !
By BioStar 1193 days agoMapping reads to a reference genome is an essential step in many types of genomic analysis, such as variant calling and gene expression analysis.1mb long DNA with Nanopore technology
By Jit 3098 days agoLongest read of 1mb achievements with NanoporeJRF in Bioinformatics @ Tezpur Universityn
Tezpur University: Napaam – 784 028: Assam Applications are invited for Walk-in-Interview for the following temporary positions in the MHRD sponsored Centre of Excellence under FAST project entitled “Machine Learning Research and Big Data...NanoPack: visualizing and processing long-read sequencing data
By Jit 2727 days agogithub.com - The NanoPack tools are written in Python3 and released under the GNU GPL3.0 License. The source code can be found at https://github.com/wdecoster/nanopack, together with links to separate scripts and their documentation. The scripts are compatible...SRF post in NEHU, Shillong
Dept of Biochemistry North-Eastern Hill University Umshing, Shillong- 793 022 Applications are invited for the post of Senior Research Fellow- SRF (one) and Junior Research Fellow- JRF (one) to be appointed in a SERB-funded major research...Kevler: Reference-free variant discovery in large eukaryotic genomes
By Jit 2329 days agogithub.com - Welcome to kevlar, software for predicting de novo genetic variants without mapping reads to a reference genome! kevlar's k-mer abundance based method calls single nucleotide variants (SNVs), multinucleotide variants (MNVs),...RA Bioinformatics at Alagappa University
RA Bioinformatics Eligibility : MSc(Bio-Chemistry, Bio-Informatics, Bio-Tech) Location : Chennai Last Date : 20 Aug 2015 Hiring Process : Walk - In Alagappa University - Job Details RA Bioinformatics Job position in Alagappa...SCUBAT: Scaffolding Contigs Using Blat And Transcripts
By Rahul Nayak 3014 days agogithub.com - SCUBAT (Scaffolding Contigs Using BLAT And Transcripts) uses any set of transcripts to identify cases where a transcript is split over multiple genome fragments and attempts to use this information to scaffold the genome.
