Results for "Structure Variation"
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Next Generation Sequencing (NGS) Tutorials
Institute of computational biomedicine, Cornell University...sis pipelines Detecting and annotating genetic variations using the HugeSeq pipeline&n...p; 10.1186/1471-2164-12-285 A framework for variation discovery and genotyping usin...3477 days ago
A Brief Bioinformatics Tutorial
This is about how to use a computer to find what is known about a gene of interest and also how to get new insights a...gnment of the homologues you've selected and how to edit this alignment. The Structure...3627 days ago
7th International Conference on Bioinformatics and Computational Biology (BICoB)
In recent years, computational biology and medical informatics have seen significant advances driven by computational...biological methods, population genetics. Structural Bioinformatics: Structure...3489 days ago
Junk part of the human genome unlocked
More: Texas A&M Biologists Unlock Non-Coding Half of Human Genome with Novel DNA S...proach to Reveal Naturally Occurring and Mutation-Induced Repetitive Sequence Variation on the Drosophila Y Chromosom...3486 days ago
- Explore genetic variation interactively. Compare entire cohorts in seconds with SQ...ith just a little code. Use Google's infrastructure and big data expertise. Store...e Genomics and take advantage of the same infrastructure that powers Search,...
3416 days ago
- ShRec3D is a program that aims at reconstructing a genome 3D structure (b) from the sole knowledge of the contacts between different genomic regions (a) as determined by Hi-C (http://ww...
3408 days ago
Resolving the complexity of the human genome using single-molecule sequencing
The human genome is arguably the most complete mammalian re...romatic gaps remain and aspects of its structural variation remain poorly understood ten...ter complexity of the human genome in the form of variation of longer and more complex re...3211 days ago
- Pilon is a software tool which can be used to: Automatically improve draft assemblies Find variation among strains, including larg...
2999 days ago
- ...e Genome Biology Group at the Broad Institute. It provides basic data structures for efficient data manipulation (mostly genomic sequences, alignments, variation etc.), as well as specialized...
2998 days ago
mrFAST: Micro Read Fast Alignment Search Tool
mrFAST is a read mapper that is designed to map short reads to reference genome with a special emphasis on the discovery of structural variation and segmental duplications. m...2921 days ago
