|
Please cite: Xia J, Wang Q, Jia P, Wang B, Pao W, Zhao Z (2012) NGS Catalog: A database of next
generation sequencing studies in humans. Human Mutation 33:E2341-2355 PubMed
Brief release history
| 9/19/2012: An indel detection tool SplazerS added to the Software page. |
| 8/22/2012: The method nFuse uploaded by an user was moved to the Software page. |
| 8/15/2012: Documents of the NGS Catalog updated. |
| 8/10/2012: One paper uploaded into the Catalog by an user was updated. |
| 7/24/2012: The software for the detection of SNVs updated. |
| 7/9/2012: 29 more papers were uploaded into the Catalog. |
| 7/3/2012: 15 recently published papers were uploaded into the Catalog. |
| 6/29/2012: The software for the detection of structural variants and gene fusions updated. |
| 1/30/2012: The mutation list of each study was uploaded into the Catalog. |
| 1/26/2012: 114 more studies were uploaded into the Catalog. |
| 11/11/2011: Eight studies were uploaded into the Catalog. |
| 8/12/2011: User manual and other documentations updated. |
| 8/11/2011: Software CREST and Avadis added. |
| 8/9/2011: Release with update of WGS. |
Copyright 2008-Present - The University of Texas Health Science Center at Houston (UTHealth)
Web File Viewing | How to Report, Fraud, Waste and Abuse | State of Texas | Statewide Search | Texas Homeland Security | Site Policies