Adam C. Siepel: History
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  • comparative genomics
  • evolutionarily
  • statistical methods

Basic Information

Adam C. Siepel
Name: Adam C. Siepel
(Jun 1972–）
Birth
Location: United States
Title: Computational biologist
Affiliations: Simons Center for Quantitative Biology Watson School for Biological Sciences
Honor: Unknown

1. Introduction

Adam C. Siepel (born 1972) is an American computational biologist known for his research in comparative genomics and population genetics, particularly the development of statistical methods and software tools for identifying evolutionarily conserved sequences.[1][2][3][4] Siepel is currently Chair of the Simons Center for Quantitative Biology and Professor in the Watson School for Biological Sciences at Cold Spring Harbor Laboratory.[5]

2. Education and Career

Siepel completed a B.S. in Agricultural and Biological Engineering at Cornell University in 1994, then worked at Los Alamos National Laboratory until 1996. From 1996 to 2001, he worked as a software developer at the National Center for Genome Resources in Santa Fe, while completing an M.S. in Computer Science at the University of New Mexico. He obtained a Ph.D. in Computer Science from the University of California, Santa Cruz in 2005. He was on the faculty of Cornell University from 2006 to 2014 and moved to Cold Spring Harbor Laboratory in 2014.

3. Research

Siepel has worked on various problems at the intersection of computer science, statistics, evolutionary biology, and genomics. At Los Alamos National Laboratory, he developed phylogenetic methods for detecting recombinant strains of HIV,[6] and at the National Center for Genome Resources, he led the development of ISYS, a technology for integrating heterogeneous bioinformatics databases, analysis tools, and visualization programs.[7] Siepel also did theoretical work on algorithms for phylogeny reconstruction based on genome rearrangements, working with Bernard Moret at the University of New Mexico.[8] When Siepel left software development to join David Haussler's laboratory at the University of California, Santa Cruz, he turned to computational problems in comparative genomics. In Haussler's group, he developed several analysis methods based on phylogenetic hidden Markov models, including a widely used program called phastCons for identifying evolutionarily conserved sequences in genomic sequences.[9]

At Cornell, Siepel's research group continued to work on the identification and characterization of conserved non-coding sequences. They also studied fast-evolving sequences in both coding[10] and noncoding[11] regions, including human accelerated regions. In recent years, the Siepel laboratory has increasingly focused on human population genetics, developing methods for estimating the times in early human history when major population groups first diverged,[12] for measuring the influence of natural selection on transcription factor binding sites,[13] and for estimating probabilities that mutations across the human genome will have fitness consequences.[14] The group also has an active research program in transcriptional regulation, carried out in close collaboration with John T. Lis's laboratory.

A common theme in Siepel's research is the development of precise mathematical models for the complex processes by which genomes evolve over time. His research group uses these models, together with techniques from computer science and statistics, both to peer into the past, and to address questions of practical importance for human health.[15]

4. Awards and Honours

Siepel was a recipient of a Guggenheim Fellowship in 2012.[15] He was also awarded a David and Lucile Packard Fellowship for Science and Engineering in 2007, a Microsoft Research Faculty Fellowship in 2007, and a Sloan Research Fellowship in 2009.

The content is sourced from: https://handwiki.org/wiki/Biography:Adam_C._Siepel

Further Reading
In this part, we encourage you to list the link of papers wrote by the character, or published reviews/articles about his/her academic contributions.

References

  1. Adam C. Siepel publications indexed by Google Scholar https://scholar.google.com/citations?user=GfQ7oQkAAAAJ
  2. Adam C. Siepel's publications indexed by the Scopus bibliographic database. (Subscription content?) https://www.scopus.com/authid/detail.url?authorId=6701428520
  3. Brian Couger, M.; Pipes, L.; Squina, F.; Prade, R.; Siepel, A.; Palermo, R.; Katze, M. G.; Mason, C. E. et al. (2014). "Enabling large-scale next-generation sequence assembly with Blacklight". Concurrency and Computation: Practice and Experience 26 (13): 2157–2166. doi:10.1002/cpe.3231. PMID 25294974.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4185199
  4. ENCODE Project Consortium, Birney E, Stamatoyannopoulos JA, Dutta A, Guigó R, Gingeras TR, Margulies EH, Weng Z, Snyder M, Dermitzakis ET (2007). "Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project". Nature 447 (7146): 799–816. doi:10.1038/nature05874. PMID 17571346. Bibcode: 2007Natur.447..799B.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2212820
  5. Adam Siepel's CV. http://siepellab.labsites.cshl.edu
  6. Siepel, A. C.; Halpern, A. L.; MacKen, C; Korber, B. T. (1995). "A computer program designed to screen rapidly for HIV type 1 intersubtype recombinant sequences". AIDS Research and Human Retroviruses 11 (11): 1413–6. doi:10.1089/aid.1995.11.1413. PMID 8573400. https://zenodo.org/record/1235237. 
  7. Siepel, A.; Farmer, A.; Tolopko, A.; Zhuang, M.; Mendes, P.; Beavis, W.; Sobral, B. (2001). "ISYS: A decentralized, component-based approach to the integration of heterogeneous bioinformatics resources". Bioinformatics 17 (1): 83–94. doi:10.1093/bioinformatics/17.1.83. PMID 11222265.  https://dx.doi.org/10.1093%2Fbioinformatics%2F17.1.83
  8. Siepel, A. C. (2003). "An algorithm to enumerate sorting reversals for signed permutations". Journal of Computational Biology 10 (3–4): 575–97. doi:10.1089/10665270360688200. PMID 12935346. http://compgen.bscb.cornell.edu/~acs/asr-jcb.pdf. 
  9. Siepel, A.; Bejerano, G; Pedersen, J. S.; Hinrichs, A. S.; Hou, M; Rosenbloom, K; Clawson, H; Spieth, J et al. (2005). "Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes". Genome Research 15 (8): 1034–50. doi:10.1101/gr.3715005. PMID 16024819.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1182216
  10. Kosiol, C.; Vinař, T. Š.; Da Fonseca, R. R.; Hubisz, M. J.; Bustamante, C. D.; Nielsen, R.; Siepel, A. (2008). "Patterns of Positive Selection in Six Mammalian Genomes". PLoS Genetics 4 (8): e1000144. doi:10.1371/journal.pgen.1000144. PMID 18670650.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2483296
  11. Pollard, K. S.; Hubisz, M. J.; Rosenbloom, K. R.; Siepel, A. (2009). "Detection of nonneutral substitution rates on mammalian phylogenies". Genome Research 20 (1): 110–21. doi:10.1101/gr.097857.109. PMID 19858363.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2798823
  12. Gronau, I.; Hubisz, M. J.; Gulko, B.; Danko, C. G.; Siepel, A. (2011). "Bayesian inference of ancient human demography from individual genome sequences". Nature Genetics 43 (10): 1031–4. doi:10.1038/ng.937. PMID 21926973.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3245873
  13. Arbiza, L.; Gronau, I.; Aksoy, B. A.; Hubisz, M. J.; Gulko, B.; Keinan, A.; Siepel, A. (2013). "Genome-wide inference of natural selection on human transcription factor binding sites". Nature Genetics 45 (7): 723–729. doi:10.1038/ng.2658. PMID 23749186.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3932982
  14. Gulko, B.; Hubisz, M. J.; Gronau, I.; Siepel, A. (2015). "A method for calculating probabilities of fitness consequences for point mutations across the human genome". Nature Genetics 47 (3): 276–283. doi:10.1038/ng.3196. PMID 25599402.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4342276
  15. Guggenheim profile. http://www.gf.org/fellows/17309-adam-siepel
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