Rahul Nayak
A Bioinformatician
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segemehl
By Anjana 3679 days agohoffmann.bioinf.uni-leipzig.de - segemehl is a software to map short sequencer reads to reference genomes. Unlike other methods, segemehl is able to detect not only mismatches but also insertions and deletions. Furthermore, segemehl is not limited to a specific read length and is...WgSim
By Jit 3635 days agogithub.com - Reads simulator Wgsim is a small tool for simulating sequence reads from a reference genome. It is able to simulate diploid genomes with SNPs and insertion/deletion (INDEL) polymorphisms, and simulate reads with uniform substitution sequencing...ART: Set of Simulation Tools
By Jit 3502 days agowww.niehs.nih.gov - ART is a set of simulation tools to generate synthetic next-generation sequencing reads. ART simulates sequencing reads by mimicking real sequencing process with empirical error models or quality profiles summarized from large recalibrated...Krona
By Jit 3363 days agogithub.com - Krona allows hierarchical data to be explored with zooming, multi-layered pie charts. Krona charts can be created using an Excel template or KronaTools, which includes support for several bioinformatics tools and raw data formats. The interactive...BBTools for bioinformatician !
By Surabhi Chaudhary 3032 days ago Comments (1)BBTools can do almost everything now !BASE: a practical de novo assembler for large genomes using long NGS reads
By Rahul Nayak 2787 days agogithub.com - new de novo assembler called BASE. It enhances the classic seed-extension approach by indexing the reads efficiently to generate adaptive seeds that have high probability to appear uniquely in the genome. Such seeds form the basis for BASE...Common steps for reads mapping !
By BioStar 1185 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.AlignGraph: algorithm for secondary de novo genome assembly guided by closely related references
By Manisha Mishra 2971 days agogithub.com - AlignGraph is a software that extends and joins contigs or scaffolds by reassembling them with help provided by a reference genome of a closely related organism. Using AlignGraph AlignGraph --read1 reads_1.fa --read2 reads_2.fa --contig contigs.fa...Converting a VCF into a FASTA given some reference !
By Jit 2878 days agoconverting a VCF file into a FASTA file given a reference sequenceQUAST-LG: Versatile genome assembly evaluation
By Jit 2781 days agocab.spbu.ru - QUAST-LG-a tool that compares large genomic de novo assemblies against reference sequences and computes relevant quality metrics. Since genomes generally cannot be reconstructed completely due to complex repeat patterns and low coverage regions, we...
