Results for "Big data"
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NGS data are just a bunch of sequences, you have no idea which region in...ce sequence is called mapping. The most used mappers of DNA-seq data are BWA and Bowtie for DNA-Seq data and Tophat, STAR&nb...2614 days ago
- FASTQ format is a text-based format for storing both a biological se...rust Sanger Institute to bundle a FASTA sequence and its quality data, but has recently become the&...
2614 days ago
- SSPACE standard is a stand-alone program f...ssembled contigs using NGS paired-read data. It is unique in offering the...ormation of paired-end and/or matepair data, SSPACE is able to assess the...a command-line tool in Perl. The input data is given by pre-assembled con...
2612 days ago
- This tutorial will serve as an example of how to use fre...e high quality assemblies of bacterial sequence data. The bacterial sample used in... as “Species” since it is live data. This data is paired-end data...
2612 days ago
A Post-assembly genome-improvement toolkit (PAGIT) to obtain annotated genomes from contigs
PAGIT addresses the need for software to generate high quality draft genomes. It is...ose gaps left open by the assembler in a draft genome, even when using the same data sets as used by the original...2604 days ago
CABOG: Celera Assembler with Best Overlap Graph
CABOG (Celera Assembler with Best Overlap Graph) is scientific software for...crobes, 2006). Today, CABOG is one of the leading assembly programs for data sets that include paired end data from the Roche 454 line of se...2602 days ago
NCBI Prokaryotic Genome Annotation Pipeline
NCBI Prokaryotic Genome Annotation Pipeline is designed...raded version that is capable of processing a larger data volume. You can find a more d...BI's annotation pipeline depends on several internal databases and is not currently ava...2600 days ago
CAR: Reconstructing Contiguous Regions of an Ancestral Genome
We describe a new method for predicting the ancestral...pecies. We combine the results from this method with data from chromosome painting expe...nts for 96.8% of the available human genome sequence data. The precision is further inc...2599 days ago
Artificial Intelligence Material !
Major Machine Learning Types Explianed in 11 Pages Credit: McKinsey For more applied resource you can see at: 1. Data Science Process https://lnkd.in/fMHtxYP 2. Data Visualization in Business htt...1792 days ago
Pollux: platform independent error correction of single and mixed genomes
Pollux: General-purpose error corrector that corrects er...logies and can be applied to single- or mixed-genome data. In addition to correcting su...verage areas of sequencing projects. Using published data sets, we correct 94% of Illum...2597 days ago
