Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Karthik Raja Velmurugan"'
Autor:
Delasa Aghamirzaie, Karthik Raja Velmurugan, Shuchi Wu, Doaa Altarawy, Lenwood S. Heath, Ruth Grene
Publikováno v:
F1000Research, Vol 6 (2017)
Motivation: The increasing availability of chromatin immunoprecipitation sequencing (ChIP-Seq) data enables us to learn more about the action of transcription factors in the regulation of gene expression. Even though in vivo transcriptional regulatio
Externí odkaz:
https://doaj.org/article/cb83b3d0d09148e086ef813abdfd51e0
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Fanconi anemia (FA) affects only one in 130,000 births, but has severe and diverse clinical consequences. It has been theorized that defects in the FA DNA cross‐link repair complex lead to a spectrum of variants that are responsible for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54adf7ff4084ea5e12eeac687a67fd3c
https://doi.org/10.1002/mgg3.502
https://doi.org/10.1002/mgg3.502
Publikováno v:
Oncogene
There remains a large discrepancy between the known genetic contributions to cancer and that which can be explained by genomic variants, both inherited and somatic. Recently, understudied repetitive DNA regions called microsatellites have been identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7e87c179aae008ee6c572012f37b59a
https://doi.org/10.1038/onc.2017.256
https://doi.org/10.1038/onc.2017.256
Autor:
Lenwood S. Heath, Karthik Raja Velmurugan, Ruth Grene, Doaa Altarawy, Delasa Aghamirzaie, Shuchi Wu
Publikováno v:
F1000Research
Motivation: The increasing availability of chromatin immunoprecipitation sequencing (ChIP-Seq) data enables us to learn more about the action of transcription factors in the regulation of gene expression. Even though in vivo transcriptional regulatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::627ae14ba09c1869fbfc3645ac4d865a
http://europepmc.org/articles/PMC5414811
http://europepmc.org/articles/PMC5414811
Autor:
Hongseok Tae, Zalman Vaksman, Karthik Raja Velmurugan, Lauren J. McIver, Harold R. Garner, Natalie C. Fonville
Publikováno v:
Scientific Reports
The human genome is 99% complete. This study contributes to filling the 1% gap by enriching previously unknown repeat regions called microsatellites (MST). We devised a Global MST Enrichment (GME) kit to enrich and nextgen sequence 2 colorectal cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23744b140854003b8172e47eeb5ad163
Publikováno v:
Advances in Bioinformatics, Vol 2015 (2015)
Advances in Bioinformatics
Advances in Bioinformatics
The emerging genome-wide hairpin bisulfite sequencing (hairpin-BS-Seq) technique enables the determination of the methylation pattern for DNA double strands simultaneously. Compared with traditional bisulfite sequencing (BS-Seq) techniques, hairpin-B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a0d1f864d4ced4d30d70c5f791a7a9f
https://doaj.org/article/d3bc0d52558b4ae99a54d9470a0c14c4
https://doaj.org/article/d3bc0d52558b4ae99a54d9470a0c14c4
Publikováno v:
Cancer Research. 77:553-553
There remains a large discrepancy between the known genetic contributions to cancer and that which can be explained by genomic variants, both inherited and somatic. Recently, understudied repetitive DNA regions called microsatellites have been identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f683e80fd23861043b763af802216b28
https://doi.org/10.1158/1538-7445.am2017-553
https://doi.org/10.1158/1538-7445.am2017-553