Results for "complete"
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Flye: Fast and accurate de novo assembler for single molecule sequencing reads
...ologies. It is designed for a wide range of datasets, from small bacterial projects to large mammalian-scale assemblies. The package represents a complete pipeline: it takes raw PB / O...1864 days ago
Flye: Fast and accurate de novo assembler for single molecule sequencing reads
...ologies. It is designed for a wide range of datasets, from small bacterial projects to large mammalian-scale assemblies. The package represents a complete pipeline: it takes raw PB / O...1770 days ago
ProteoClade: A taxonomic toolkit for multi-species and metaproteomic analysis
...reference database (ex: using PEAKS, PepNovo). ProteoClade scales from two organisms to every organism in UniProt. Please refer to the complete documentation at proteoclade....1513 days ago
CSAR-web: a web server of contig scaffolding using algebraic rearrangements
...order and orient) the contigs of a target draft genome based on a complete or incomplete reference genome from a relat...ciently and accurately scaffold their draft genomes according to a complete or incomplete reference genom...1491 days ago
HS3D: Homo Sapiens Splice Sites Dataset
...onal approaches for gene identification and characterization. From the complete GenBank (Primate Sequences Di...ion) Rel.123 (162,557 entries), entries of Human Nuclear DNA including Complete CDS and more than one Exon ha...1427 days ago
LR_Gapcloser: a tiling path-based gap closer that uses long reads to complete genome assembly
LR_Gapcloser is a gap closing tool using long reads from studied species. The long reads could be downloaed from public read archive database (for instance, NCBI SRA dat...1456 days ago
- ...g chromatin interaction data, you can also seamlessly browse other omics data such as ChIP-Seq or RNA-Seq for the same genomic region, and gain a complete view of both regulatory lands...
1203 days ago
QuasR: Quantification and annotation of short reads in R
...ents, starting from the raw sequence reads, over pre-processing and alignment, up to quantification. A single R script can contain all steps of a complete analysis, making it simple to...1001 days ago
The complete sequence of a human genome
The completed regions include all centromeric satellite arrays, recent segmental duplications, and the short arms of all five acrocentric chromosomes, unlocking these complex regions of the genome to variational and functional studies.770 days ago
Merfin: improved variant filtering, assembly evaluation and polishing via k-mer validation
...ies built from Pacific Biosciences HiFi and continuous long reads or Oxford Nanopore reads, including the first complete human genome. Moreover, we introduce assembly quality and completeness metrics that account for...767 days ago
