Abhimanyu Singh
A bioinformatics beginner
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LSC: Improving PacBio Long Read Accuracy by Short Read Alignment
By Abhimanyu Singh 2268 days agowww.healthcare.uiowa.edu - Added Command line argument support. Multi-stage execution modes. Support for parallelization. Now execution proceeds in batches of long reads the size of which can be set by --long_read_batch_size N. Better compressed intermediate files. Added...Encode sequencing data freely available to download and use for academic means
By Rahul Agarwal 3906 days ago Comments (3)genome.ucsc.edu - In Encode, regulatory elements investigated via DNA hypersensitivity assays, assays of DNA methylation, and chromatin immunoprecipitation (ChIP) of proteins that interact with DNA, including modified histones and transcription factors, followed...Calling narrow and broad peaks from ChIP-Seq data
By Strand 3398 days agoCalling narrow and broad peaks from ChIP-Seq dataMetaGraph: Ultra Scalable Framework for DNA Search, Alignment, Assembly
By Abhi 166 days agometagraph.ethz.ch - The MetaGraph framework is designed to work with a wide range of input data sets, indexing from a few samples up to the contents of entire archives with hundreds of thousands of records. The indexing workflow always follows the same principle,...repeat-aware: Repeat aware scaffolding evaluation framework by Igor Mandric
By Jit 2437 days agogithub.com - Genome scaffolding is a classical challenging problem in bioinformatics. It refers to joining assembly contigs into chains (called scaffolds). The join between two contigs A and B is considered correct if: Their relative orientation is...nQuire: A statistical framework for ploidy estimation using NGS short-read data
By Jit 2122 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...UniAligner: a parameter-free framework for fast sequence alignment
By Abhi 258 days agogithub.com - UniAligner (formerly, TandemAligner) is the first parameter-free algorithm for sequence alignment that introduces a sequence-dependent alignment scoring that automatically changes for any pair of compared sequences. Classical alignment approaches,...Grinder / Biogrinder - A versatile omics shotgun and amplicon sequencing read simulator
By Jit 2739 days agosourceforge.net - Grinder is a versatile program to create random shotgun and amplicon sequence libraries based on DNA, RNA or proteic reference sequences provided in a FASTA file. Grinder can produce genomic, metagenomic, transcriptomic, metatranscriptomic,...LRCstats: Long Read Correction Statistics
By Jit 2513 days agogithub.com - LRCstats is an open-source pipeline for benchmarking DNA long read correction algorithms for long reads outputted by third generation sequencing technology such as machines produced by Pacific Biosciences. The reads produced by third generation...SISRS: Site Identification from Short Read Sequences
By Abhimanyu Singh 2186 days agogithub.com - Next-gen sequence data such as Illumina HiSeq reads. Data must be sorted into folders by taxon (e.g. species or genus). Paired reads in fastq format must be specified by _R1 and _R2 in the (otherwise identical) filenames. Paired and unpaired reads...
