Results for "Multiple"
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A Brief Bioinformatics Tutorial
...w to look efficiently for a particular protein sequence, how to blast it against the database of your choice to find homologues, how to perform a multiple alignment of the homologues y...3621 days ago
- ...las, ArrayExpress, and PIPAx database. As for the analytics, there is gene selection, quality control, scoring distances between experiments with multiple factors. All features can be...
3483 days ago
7th International Conference on Bioinformatics and Computational Biology (BICoB)
... Genome assembly, genome annotation, gene finding, alternative splicing, EST analysis and comparative genomics. Sequence analysis: Multiple sequence alignment, sequence...3482 days ago
- ...or hours, by using parallel computing frameworks like MapReduce. Explore data by slicing alignments and variants by genomic range across one or multiple samples -- for your own algor...
3472 days ago
- HapSolo, that identifies secondary contigs and defines a primary assembly based on multiple pairwise contig alignment metrics. HapSolo evaluates candidate primary assemblies using BUSC...
1076 days ago
Alignment of closely related whole genomes/scaffolds
...se in the number of sequenced genomes for species across the tree of life. This increasing volume of data requires tools that can quickly compare multiple whole-genome sequences, milli...3003 days ago
- ...The Bio::ToolBox libraries provide a unified, abstracted interface to multiple common gene annotation formats and the collection of data from multiple data files. They rely on BioP...
2982 days ago
Ensembl comparative genomics resources
...ources are one such reference set that facilitates comprehensive and reproducible analysis of chordate genome data. Ensembl computes pairwise and multiple whole-genome alignments from...2972 days ago
- ...paired-end sequencing data. Users could ran it easily by just alling SVelter.py with proper parameters. It's also possible to ran it on multiple cores by calling different su...
2971 days ago
- Destruct is a tool for joint prediction of rearrangement breakpoints from single or multiple tumour samples. More at https://bitbucket.org/dranew/destruct
2971 days ago
