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Broadly Accessible Technologies for Single-cell Joint Analysis of Transcriptome and Epigenome

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R41MH128993-01
Agency Tracking Number: R41MH128993
Amount: $894,953.00
Phase: Phase I
Program: STTR
Solicitation Topic Code: 101
Solicitation Number: PA20-265
Timeline
Solicitation Year: 2020
Award Year: 2022
Award Start Date (Proposal Award Date): 2022-09-01
Award End Date (Contract End Date): 2024-08-31
Small Business Information
9853 Pacific Heights Blvd. Suite G&H
San Diego, CA 92121
United States
DUNS: 117647710
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 BING REN
 (858) 822-5766
 biren@ucsd.edu
Business Contact
 PEI LIN
Phone: (858) 344-1618
Email: peilin9@gmail.com
Research Institution
 UNIVERSITY OF CALIFORNIA, SAN DIEGO
 
OFFICE OF CONTRACT & GRANT ADMIN 9500 GILMAN DRIVE 0934
LA JOLLA, CA 92093-0621
United States

 Nonprofit College or University
Abstract

AbstractHistone modifications carry rich information of cellular memory and gene regulatory mechanisms. Single cell
analysis of histone modification in conjunction with transcriptome could recover this critical layer of cell identity
and help to dissect the cellular and molecular composition of complex tissues such as the brain. We recently
developed an ultra-high throughput single cell multi-omics assay, Paired-Tag, that can jointly map transcriptome
and histone modifications from up to a million single cells in parallel. In order to translate this novel technology
to the marketplace and to advance the goals of the BRAIN initiative, we propose to optimize and further develop
Paired-Tag to enable its broad use in the research community. Specifically, we will develop Paired-Tag kits to
allow for general accessibility of the method in molecular biology laboratories. We will then carry out extensive
field tests of the Paired-Tag kit in the laboratories of current BRAIN initiative investigators, and further improve it
based on the feedbacks. Finally, we will adapt the Paired-Tag procedure to long-read sequencing technologies
to enable high throughput detection of splicing isoforms in brain cells at single cell resolution. If successful, the
proposed research would provide researchers with a powerful new tool for single cell transcriptomics and
epigenomics analysis.

* Information listed above is at the time of submission. *

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