Хайлтын үр дүнгүүд - Daniel C. Koboldt
- 57-н 1 - 20 үр дүнгүүдийг харуулж байна
- Дараагийн хуудас руу очих
-
1
Best practices for variant calling in clinical sequencing -н Daniel C. Koboldt
Хэвлэсэн 2020Revisão -
2
-
3
-
4
Challenges of sequencing human genomes -н Daniel C. Koboldt, Li Ding, Elaine R. Mardis, Rick K. Wilson
Хэвлэсэн 2010Revisão -
5
-
6
-
7
Comparison of C. elegans and C. briggsae Genome Sequences Reveals Extensive Conservation of Chromosome Organization and Synteny -н LaDeana Hillier, Raymond D. Miller, Scott E. Baird, Asif Chinwalla, Lucinda A. Fulton, Daniel C. Koboldt, R Waterston
Хэвлэсэн 2007Artigo -
8
Caenorhabditis briggsae Recombinant Inbred Line Genotypes Reveal Inter-Strain Incompatibility and the Evolution of Recombination -н Joseph A. Ross, Daniel C. Koboldt, Julia Staisch, Helen Chamberlin, Bhagwati P. Gupta, Raymond D. Miller, Scott E. Baird, Eric S. Haag
Хэвлэсэн 2011Artigo -
9
-
10
SomaticSniper: identification of somatic point mutations in whole genome sequencing data -н David E. Larson, Christopher Harris, Ken Chen, Daniel C. Koboldt, Travis E. Abbott, David J. Dooling, Timothy J. Ley, Elaine R. Mardis, Richard K. Wilson, Li Ding
Хэвлэсэн 2011Artigo -
11
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing -н Daniel C. Koboldt, Qunyuan Zhang, David E. Larson, Dong Shen, Michael D. McLellan, Ling Lin, Christopher A. Miller, Elaine R. Mardis, Li Ding, Richard K. Wilson
Хэвлэсэн 2012Artigo -
12
MuSiC: Identifying mutational significance in cancer genomes -н Nathan D. Dees, Qunyuan Zhang, Cyriac Kandoth, Michael C. Wendl, William Schierding, Daniel C. Koboldt, Thomas B. Mooney, Matthew B. Callaway, David J. Dooling, Elaine R. Mardis, Richard K. Wilson, Li Ding
Хэвлэсэн 2012Artigo -
13
CMDS: a population-based method for identifying recurrent DNA copy number aberrations in cancer from high-resolution data -н Qunyuan Zhang, Li Ding, David E. Larson, Daniel C. Koboldt, Michael D. McLellan, Ken Chen, Xiaoqi Shi, Aldi T. Kraja, Elaine R. Mardis, Richard K. Wilson, Ingrid B. Borecki, Michael A. Province
Хэвлэсэн 2009Artigo -
14
Activating HER2 Mutations in HER2 Gene Amplification Negative Breast Cancer -н Ron Bose, Shyam M. Kavuri, Adam C. Searleman, Wei Shen, Dong Shen, Daniel C. Koboldt, John Monsey, Nicholas Goel, Adam B. Aronson, Shunqiang Li, X. Cynthia, Li Ding, Elaine R. Mardis, Matthew J. Ellis
Хэвлэсэн 2012Artigo -
15
Identification of Rare Variants Predisposing to Thyroid Cancer -н Yanqiang Wang, Sandya Liyanarachchi, Katherine E. Miller, Taina T. Nieminen, Daniel F. Comiskey, Wei Li, Pamela Brock, David E. Symer, Keiko Akagi, Katherine E. DeLap, Huiling He, Daniel C. Koboldt, Albert de la Chapelle
Хэвлэсэн 2019Artigo -
16
An ensemble approach to accurately detect somatic mutations using SomaticSeq -н Li Tai Fang, Pegah Tootoonchi Afshar, Aparna Chhibber, Marghoob Mohiyuddin, Yu Fan, John C. Mu, Greg Gibeling, Sharon Barr, Narges Bani Asadi, Mark Gerstein, Daniel C. Koboldt, Wenyi Wang, Wing Hung Wong, Hugo Y. K. Lam
Хэвлэсэн 2015Artigo -
17
Identification of Disease-Causing Mutations in Autosomal Dominant Retinitis Pigmentosa (adRP) Using Next-Generation DNA Sequencing -н Sara J. Bowne, Lori S. Sullivan, Daniel C. Koboldt, Li Ding, Robert S. Fulton, Rachel M. Abbott, Erica Sodergren, David G. Birch, Dianna H. Wheaton, John R. Heckenlively, Qin Liu, Eric A. Pierce, George M. Weinstock, Stephen P. Daiger
Хэвлэсэн 2010Artigo -
18
<i>IRF6</i> mutation screening in non‐syndromic orofacial clefting: analysis of 1521 families -н Elizabeth J. Leslie, Daniel C. Koboldt, Cho Kang, Li Ma, Jacqueline T. Hecht, George L. Wehby, Kaare Christensen, Andrew E. Czeizel, Frederic W.‐B. Deleyiannis, Robert S. Fulton, Richard K. Wilson, Terri H. Beaty, Brian C. Schutte, Jeffrey C. Murray, Mary L. Marazita
Хэвлэсэн 2015Artigo -
19
Complete characterization of the microRNAome in a patient with acute myeloid leukemia -н Giridharan Ramsingh, Daniel C. Koboldt, Maria Trissal, Katherine B. Chiappinelli, Todd Wylie, Sunita Koul, Li‐Wei Chang, Rakesh Nagarajan, Todd A. Fehniger, Paul J. Goodfellow, Vincent Magrini, Richard K. Wilson, Li Ding, Timothy J. Ley, Elaine R. Mardis, Daniel C. Link
Хэвлэсэн 2010Artigo -
20
Next-generation sequencing identifies the natural killer cell microRNA transcriptome -н Todd A. Fehniger, Todd Wylie, Elizabeth Germino, Jeffrey Leong, Vincent Magrini, Sunita Koul, Catherine R. Keppel, Stephanie Schneider, Daniel C. Koboldt, Ryan P. Sullivan, Michael Heinz, Seth D. Crosby, Rakesh Nagarajan, Giridharan Ramsingh, Daniel C. Link, Timothy J. Ley, Elaine R. Mardis
Хэвлэсэн 2010Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Genetics
Gene
Mutation
Cancer research
Computational biology
Genome
Cancer
Exome sequencing
Medicine
Germline mutation
Computer science
DNA sequencing
Exome
Somatic cell
Genotype
Missense mutation
Myeloid leukemia
Allele
Gene expression
Germline
Myeloid
Phenotype
Single-nucleotide polymorphism
DNA methylation
Evolutionary biology
Immunology
Massive parallel sequencing
Neuroscience
Artificial intelligence