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Apollo: First instantaneous, collaborative genomic annotation editor available on the Web
By Jit 2004 days agogenomearchitect.github.io - Apollo is a plug-in for the JBrowse Genome Viewer. In addition to genes and pseudogenes, users can annotate ncRNAs (snRNA, snoRNA, tRNA, rRNA), miRNAs, repeat regions, and transposable elements; each annotation type has its own...simuG: a general-purpose genome simulator
By BioStar 1824 days agogithub.com - Simulated genomes with pre-defined and random genomic variants can be very useful for benchmarking genomic and bioinformatics analyses. Here we introduce simuG, a lightweight tool for simulating the full-spectrum of genomic variants (single...China’s BGI says it can sequence a genome for just $100
By Neel 1731 days ago Comments (6)China’s BGI says it can sequence a genome for just $100RefKA: A fast and efficient long-read genome assembly approach for large and complex genomes
By Rahul Nayak 1669 days agogithub.com - RefKA, a reference-based approach for long read genome assembly. This approach relies on breaking up a closely related reference genome into bins, aligning k-mers unique to each bin with PacBio reads, and then assembling each bin in parallel...merqury: Evaluate genome assemblies with k-mers
By Jit 1605 days agogithub.com - Often, genome assembly projects have illumina whole genome sequencing reads available for the assembled individual. The k-mer spectrum of this read set can be used for independently evaluating assembly quality without the need of a high quality...Ancient whole genome duplication (WGD) detection tools !
By Rahul Nayak 1359 days agoThere are two methods for ancient WGD detection, one is collinearity analysis, and the other is based on the Ks distribution map. Among them, Ks is defined as the average number of synonymous substitutions at each synonymous site, and there is...Calling variants in non-diploid systems
By Neel 1247 days ago Comments (1)training.galaxyproject.org - The main challenge associated with non-diploid variant calling is the difficulty in distinguishing between the sequencing noise (abundant in all NGS platforms) and true low frequency variants. Some of the early attempts to do this well have been...KAU Thrissur Biotech/Bioinformatics RA/SRF/JRF/Trainee/Studentships
Applications are invited from eligible candidates for the following posts at Bioinformatics Centre (DIC), IT- BT Complex, College of Horticulture, Kerala Agricultural University, Vellanikkara, Thrissur. 1. Research Associate Emoluments*:...GenomeTools: The versatile open source genome analysis software
By Neel 1027 days agohttp://genometools.org/ - The GenomeTools genome analysis system is a free collection of bioinformatics tools (in the realm of genome informatics) combined into a single binary named gt. It is based on a C library named...Refseq viraal genome sequences !
By Jit 1079 days agoftp.ncbi.nlm.nih.gov - List of all viruses on NCBI https://ftp.ncbi.nlm.nih.gov/refseq/release/viral/
