Jit
Enthusiast computational biologist with business dream !!!
Our Sponsors
Related items
Bioinformatics and Sequencing Courses and Workshops
Last updated 4791 days ago by Rahul Agarwal Comments (2)Swiss Institute of Bioinformatics (SIB) organises lots of bioinformatics courses covering wide range of topics: http://www.isb-sib.ch/education/training-courses.html Canadian bioinformatics also organises various bioinformatics and sequencing...Uni Computing Bergen Norway
Info on Uni Computing (Webpage: http://www.bccs.uni.no/) : Uni Computing (formerly Uni BCCS) is a department of Uni Research, affiliated with the University of Bergen. 5 groups in this lab works on computational resources, methods, algorithms,...Bioinformatics job in Genotypic Tech, India
Genotypic Technology, the first Genomics Company of India is poised to become the next generation life sciences company. We are hiring professionals for our high end Genomics Labs (Molecular Biology/ Microarray/NGS) and Bioinformatics...Flye: Fast and accurate de novo assembler for single molecule sequencing reads
By Jit 3077 days agogithub.com - Flye is a de novo assembler for long and noisy reads, such as those produced by PacBio and Oxford Nanopore Technologies. The algorithm uses an A-Bruijn graph to find the overlaps between reads and does not require them to be error-corrected. After...FinisherSC:a repeat-aware tool for upgrading de novo assembly using long reads
By Jit 2970 days agogithub.com - Here is the command to run the tool: python finisherSC.py destinedFolder mummerPath If you are running on server computer and would like to use multiple threads, then the following commands can generate 20 threads to run FinisherSC. python...P_RNA_scaffolder: a fast and accurate genome scaffolder using paired-end RNA-sequencing reads
By BioStar 2952 days agowww.fishbrowser.org - P_RNA_scaffolder is a novel scaffolding tool using Pair-end RNA-seq to scaffold genome fragments. The method is suitable for most genomes. The program could utilize Illumina Paired-end RNA-sequencing reads from target speciesies. Our method provides...FastProNGS: fast preprocessing of next-generation sequencing reads
By Rahul Nayak 2111 days agogithub.com - FastProNGS to integrate the quality control process with automatic adapter removal. Parallel processing was implemented to speed up the process by allocating multiple threads. Compared with similar up-to-date preprocessing tools, FastProNGS is by...Jabba: Hybrid Error Correction for Long Sequencing Reads
By Jit 3197 days agogithub.com - Jabba is a hybrid error correction tool to correct third generation (PacBio / ONT) sequencing data, using second generation (Illumina) data. Input Jabba takes as input a concatenated de Bruijn graph and a set of sequences: the de Bruijn graph...gSearch: a fast and flexible general search tool for whole-genome sequencing
By Jit 2983 days agoml.ssu.ac.kr - gSearch compares sequence variants in the Genome Variation Format (GVF) or Variant Call Format (VCF) with a pre-compiled annotation or with variants in other genomes. Its search algorithms are subsequently optimized and implemented in a...
