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...3488 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...3637 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...3499 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...3496 days ago
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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...3221 days ago
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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...2932 days ago