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Ensembl 2015
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DOI：10.1093/nar/gku1010.png)
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摘要
En 中文
Ensembl (ext-link-type=uri xlink:href=http://www.ensembl.org xlink:type=simple>http://www.ensembl.org) is a genomic interpretation system providing the most up-to-date annotations, querying tools and access methods for chordates and key model organisms. This year we released updated annotation (gene models, comparative genomics, regulatory regions and variation) on the new human assembly, GRCh38, although we continue to support researchers using the GRCh37.p13 assembly through a dedicated site (ext-link-type=uri xlink:href=http://grch37.ensembl.org xlink:type=simple>http://grch37.ensembl.org). Our Regulatory Build has been revamped to identify regulatory regions of interest and to efficiently highlight their activity across disparate epigenetic data sets. A number of new interfaces allow users to perform large-scale comparisons of their data against our annotations. The REST server (ext-link-type=uri xlink:href=http://rest.ensembl.org xlink:type=simple>http://rest.ensembl.org), which allows programs written in any language to query our databases, has moved to a full service alongside our upgraded website tools. Our online Variant Effect Predictor tool has been updated to process more variants and calculate summary statistics. Lastly, the WiggleTools package enables users to summarize large collections of data sets and view them as single tracks in Ensembl. The Ensembl code base itself is more accessible: it is now hosted on our GitHub organization page (ext-link-type=uri xlink:href=https://github.com/Ensembl xlink:type=simple>https://github.com/Ensembl) under an Apache 2.0 open source license.
Keyword:
DATABASE
SEQUENCE
CONSEQUENCES
DISCOVERY
ACCESS
API
AI总结
对已上传原文的论文进行重点信息的提取，主要内容包括：简要概述、研究摘要、背景介绍、关键亮点、图文解析、展望与总结。
期刊
IF:
13.1
论文数:
3.6W
被引数:
29.0W
机构
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