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Hong Sain Ooi

Researcher at Agency for Science, Technology and Research

Publications -  13
Citations -  7920

Hong Sain Ooi is an academic researcher from Agency for Science, Technology and Research. The author has contributed to research in topics: Chromatin immunoprecipitation & Genome. The author has an hindex of 11, co-authored 12 publications receiving 7480 citations. Previous affiliations of Hong Sain Ooi include Research Institute of Molecular Pathology & Genome Institute of Singapore.

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Journal ArticleDOI

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Ewan Birney, +320 more
- 14 Jun 2007 - 
TL;DR: Functional data from multiple, diverse experiments performed on a targeted 1% of the human genome as part of the pilot phase of the ENCODE Project are reported, providing convincing evidence that the genome is pervasively transcribed, such that the majority of its bases can be found in primary transcripts.
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Global mapping of c-Myc binding sites and target gene networks in human B cells

TL;DR: A snapshot of genome-wide, unbiased characterization of direct Myc binding targets in a model of human B lymphoid tumor using ChIP coupled with pair-end ditag sequencing analysis (ChIP-PET) provides a substantial framework for the understanding of mechanisms of Myc-induced tumorigenesis.
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ChIA-PET tool for comprehensive chromatin interaction analysis with paired-end tag sequencing

TL;DR: Chia-PET Tool, a software package for automatic processing of ChIA-PET sequence data, including linker filtering, mapping tags to reference genomes, identifying protein binding sites and chromatin interactions, and displaying the results on a graphical genome browser is presented.
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Multiplex sequencing of paired-end ditags (MS-PET): a strategy for the ultra-high-throughput analysis of transcriptomes and genomes.

TL;DR: This combined sequencing strategy achieved an approximate 100-fold efficiency increase over the current standard for PET analysis, and furthermore enables the short-read-length multiplex sequencing procedure to acquire paired-end information from large DNA fragments.