Neel
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MEC: Contig Misassembly Correction
By BioStar 1752 days agogithub.com - MEC, to identify and correct misassemblies in contigs. Firstly, MEC takes fragment coverage as the feature to detect the candidate misassemblies. Then, it can distinguish a large number of false positives from the candidate misassemblies based on...AfterQC: Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data
By Jit 2338 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...SimLoRD: A read simulator for third generation sequencing reads
By Aaryan Lokwani 2283 days agobitbucket.org - SimLoRD is a read simulator for third generation sequencing reads and is currently focused on the Pacific Biosciences SMRT error model. Reads are simulated from both strands of a provided or randomly generated reference sequence. The reference...GMcloser: closing gaps in assemblies accurately with a likelihood-based selection of contig or...
By Shruti Paniwala 2356 days agoacademic.oup.com - GMcloser uses likelihood-based classifiers calculated from the alignment statistics between scaffolds, contigs and paired-end reads to correctly assign contigs or long reads to gap regions of scaffolds, thereby achieving accurate and efficient gap...RefKA: A fast and efficient long-read genome assembly approach for large and complex genomes
By Rahul Nayak 1666 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...GraphMap - A highly sensitive and accurate mapper for long, error-prone reads
By Rahul Agarwal 3426 days ago Comments (1)github.com - GraphMap is a novel mapper targeted at aligning long, error-prone third-generation sequencing data.It is designed to handle Oxford Nanopore MinION 1d and 2d reads with very high sensitivity and accuracy, and also presents a significant...
SPAdes hybrid genome assembly
Last updated 2551 days ago by Jit Comments (1)When you have both Illumina and Nanopore data, then SPAdes remains a good option for hybrid assembly - SPAdes was used to produce the B fragilis assembly by Mick Watson’s group. Again, running spades.py will show you the...Deepbinner: a signal-level demultiplexer for Oxford Nanopore reads
By Neel 2187 days agogithub.com - Deepbinner is a tool for demultiplexing barcoded Oxford Nanopore sequencing reads. It does this with a deep convolutional neural network classifier, using many of the architectural advances that have proven successful...Now time is come to revolutionize amino acid sequencing by Nanopore technology
By Rahul Agarwal 3882 days agowww.eurekalert.org - Amino acid sequencing by Nanopore recognition tunneling method1mb long DNA with Nanopore technology
By Jit 2529 days agoLongest read of 1mb achievements with Nanopore
