Misplaced Pages

Sergey Koren

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
U.S. bioinformatician
Sergey Koren
Koren in 2023
Alma materUniversity of Maryland, College Park
Scientific career
FieldsGenome informatics
InstitutionsNational Human Genome Research Institute

Sergey Koren is an American bioinformatician who is an associate investigator in the genome informatics section at the National Human Genome Research Institute.

After completing his M.S., Koren joined the J. Craig Venter Institute (JCVI) as a bioinformatics engineer under the supervision of Granger Sutton. During his three years at JCVI, he contributed to the development of the Celera Assembler, which has been used to assemble both the Drosophila melanogaster and human genomes. In parallel, Koren worked under the supervision Mihai Pop at the University of Maryland, College Park, where he developed several tools for metagenome assembly and analysis.

In 2010, Koren joined the National Biodefense Analysis and Countermeasures Center (NBACC) where he led genome assembly development and pioneered the use of single-molecule sequencing for the reconstruction of complete genomes. In 2015, Koren joined the National Human Genome Research Institute (NHGRI) as a founding member of the genome informatics section. He is an associate investigator in the Genome Informatics Section, Computational and Statistical Genomics Branch at the National Human Genome Research Institute. In 2022, he was one of the lead authors on the publication reporting the first complete female human genome.

References

  1. ^ "Sergey Koren, Ph.D." Genome.gov. Retrieved 2023-05-28.Public Domain This article incorporates text from this source, which is in the public domain.
  2. Nurk S, Koren S, Rhie A, Rautiainen M, Bzikadze AV, Mikheenko A, Vollger MR, Altemose N, Uralsky L, Gershman A, Aganezov S, Hoyt SJ, Diekhans M, Logsdon GA, Alonge M, Antonarakis SE, Borchers M, Bouffard GG, Brooks SY, Caldas GV, Chen NC, Cheng H, Chin CS, Chow W, de Lima LG, Dishuck PC, Durbin R, Dvorkina T, Fiddes IT, Formenti G, Fulton RS, Fungtammasan A, Garrison E, Grady PG, Graves-Lindsay TA, Hall IM, Hansen NF, Hartley GA, Haukness M, Howe K, Hunkapiller MW, Jain C, Jain M, Jarvis ED, Kerpedjiev P, Kirsche M, Kolmogorov M, Korlach J, Kremitzki M, Li H, Maduro VV, Marschall T, McCartney AM, McDaniel J, Miller DE, Mullikin JC, Myers EW, Olson ND, Paten B, Peluso P, Pevzner PA, Porubsky D, Potapova T, Rogaev EI, Rosenfeld JA, Salzberg SL, Schneider VA, Sedlazeck FJ, Shafin K, Shew CJ, Shumate A, Sims Y, Smit AF, Soto DC, Sović I, Storer JM, Streets A, Sullivan BA, Thibaud-Nissen F, Torrance J, Wagner J, Walenz BP, Wenger A, Wood JM, Xiao C, Yan SM, Young AC, Zarate S, Surti U, McCoy RC, Dennis MY, Alexandrov IA, Gerton JL, O'Neill RJ, Timp W, Zook JM, Schatz MC, Eichler EE, Miga KH, Phillippy AM (April 2022). "The complete sequence of a human genome". Science. 376 (6588): 44–53. Bibcode:2022Sci...376...44N. doi:10.1126/science.abj6987. PMC 9186530. PMID 35357919. S2CID 247854936.
Public Domain This article incorporates public domain material from websites or documents of the National Institutes of Health. Categories: