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Jorja G. Henikoff

Researcher at Fred Hutchinson Cancer Research Center

Publications -  66
Citations -  21496

Jorja G. Henikoff is an academic researcher from Fred Hutchinson Cancer Research Center. The author has contributed to research in topics: Chromatin & Nucleosome. The author has an hindex of 46, co-authored 64 publications receiving 19163 citations. Previous affiliations of Jorja G. Henikoff include Memorial Sloan Kettering Cancer Center & University of Washington.

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Amino acid substitution matrices from protein blocks

TL;DR: This work has derived substitution matrices from about 2000 blocks of aligned sequence segments characterizing more than 500 groups of related proteins, leading to marked improvements in alignments and in searches using queries from each of the groups.
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Identification of Functional Elements and Regulatory Circuits by Drosophila modENCODE

Sushmita Roy, +95 more
- 24 Dec 2010 - 
TL;DR: The Drosophila Encyclopedia of DNA Elements (modENCODE) project as mentioned in this paper has been used to map transcripts, histone modifications, chromosomal proteins, transcription factors, replication proteins and intermediates, and nucleosome properties across a developmental time course and in multiple cell lines.
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Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project

Mark Gerstein, +130 more
- 24 Dec 2010 - 
TL;DR: These studies identified regions of the nematode and fly genomes that show highly occupied targets (or HOT) regions where DNA was bound by more than 15 of the transcription factors analyzed and the expression of related genes were characterized, providing insights into the organization, structure, and function of the two genomes.
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CUT&Tag for efficient epigenomic profiling of small samples and single cells

TL;DR: Cleavage Under Targets and Tagmentation (CUT&Tag), an enzyme-tethering strategy that provides efficient high-resolution sequencing libraries for profiling diverse chromatin components, is described.
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Consensus-degenerate hybrid oligonucleotide primers for amplification of distantly related sequences.

TL;DR: A new primer design strategy for PCR amplification of unknown targets that are related to multiply-aligned protein sequences that consists of a short 3' degenerate core region and a longer 5' consensus clamp region, which demonstrates the practical utility of this hybrid primer method.