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Consed--A Finishing Package (BAM File Viewer, Assembly Editor, Autofinish, Autoreport, Autoedit,...
By Neel 1756 days agowww.phrap.org - Supports Illumina, 454, other Next-Gen and Sanger Reads and allows mixtures of these read types Consed includes BamScape which can view bam files with unlimited numbers of reads. BamScape can bring up consed to edit reads and the reference sequence...Protocol for De novo Genome Assembly using Illumina Reads
By BioStar 1411 days agoIn this protocol, we address and describe the de novo assembly method for small to medium-sized genomes.
Bioinformatics Training Courses At RASA LSI
Last updated 1849 days ago by RASA Life SciencesRASA conducts comprehensive Life Science skill development training courses in Pune, India for working professionals, researchers, students and job-seeker. The trainings are crafted meticulously, covering different modules of courses such as...3rd Annual Next Generation Sequencing Asia Congress 2013 at Singapore, Singapore
The 3rd Annual Next Generation Sequencing Asia Congress is to be held on the 22nd and 23rd of October 2013 in Singapore. Over the 2 days, the conference will provide an overview of the current options of next-generation sequencing platforms,...Amity University Bioinformatics Summer Program - Kolkata
By eliabrodsky 1996 days agoRegistrations are now open for the 2019 Summer Bioinformatics Training program at Amity University, Kolkata.AfterQC: Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data
By Jit 2344 days ago Comments (1)github.com - Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data AfterQC can simply go through all fastq files in a folder and then output three folders: good, bad and QC folders, which contains good reads, bad reads and the QC...nQuire: A statistical framework for ploidy estimation using NGS short-read data
By Jit 2128 days agogithub.com - 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...BBTools for bioinformatician !
By Surabhi Chaudhary 2478 days ago Comments (1)BBTools can do almost everything now !The genome factory !!!
By Madhvan Reddy 3969 days agoWorld’s first $1,000 genome enables ‘factory’ scale sequencing for population and disease studiesUnderstanding HiFi Reads !
By Rahul Nayak 979 days agopacb.com - While little public data is available for either of the new synthetic long read approaches, Illumina showed an example comparison earlier this year at the Festival of Genomics & Biodata conference (FoG 2022). In the IGV screenshot...
