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Li Ding
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Displaying results 1-7 of
7
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:
GenomeVIP: a cloud platform for genomic variant discovery and interpretation
R. Jay Mashl
,
Adam D. Scott
,
Kuan-lin Huang
,
Matthew A. Wyczalkowski
,
Christopher J. Yoon
,
Beifang Niu
,
Erin DeNardo
,
Venkata D. Yellapantula
,
Robert E. Handsaker
,
Ken Chen
,
Daniel C. Koboldt
,
Kai Ye
,
David Fenyö
,
Benjamin J. Raphael
,
Michael C. Wendl
,
and
Li Ding
Genome Res.
August 2017
27
:
1450
-
1459
;
Published in Advance
May 18, 2017
,
doi:
10.1101/gr.211656.116
Abstract
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Method
:
TIGRA: A targeted iterative graph routing assembler for breakpoint assembly
Ken Chen
,
Lei Chen
,
Xian Fan
,
John Wallis
,
Li Ding
,
and
George Weinstock
Genome Res.
February 2014
24
:
310
-
317
;
Published in Advance
December 4, 2013
,
doi:
10.1101/gr.162883.113
Abstract
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:
Somatic neurofibromatosis type 1 (NF1) inactivation characterizes NF1-associated pilocytic astrocytoma
David H. Gutmann
,
Michael D. McLellan
,
Ibrahim Hussain
,
John W. Wallis
,
Lucinda L. Fulton
,
Robert S. Fulton
,
Vincent Magrini
,
Ryan Demeter
,
Todd Wylie
,
Cyriac Kandoth
,
Jeffrey R. Leonard
,
Abhijit Guha
,
Christopher A. Miller
,
Li Ding
,
and
Elaine R. Mardis
Genome Res.
March 2013
23
:
431
-
439
;
Published in Advance
December 5, 2012
,
doi:
10.1101/gr.142604.112
Abstract
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:
MuSiC: Identifying mutational significance in cancer genomes
Nathan D. Dees
,
Qunyuan Zhang
,
Cyriac Kandoth
,
Michael C. Wendl
,
William Schierding
,
Daniel C. Koboldt
,
Thomas B. Mooney
,
Matthew B. Callaway
,
David Dooling
,
Elaine R. Mardis
,
Richard K. Wilson
,
and
Li Ding
Genome Res.
August 2012
22
:
1589
-
1598
;
Published in Advance
July 3, 2012
,
doi:
10.1101/gr.134635.111
Abstract
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:
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
Daniel C. Koboldt
,
Qunyuan Zhang
,
David E. Larson
,
Dong Shen
,
Michael D. McLellan
,
Ling Lin
,
Christopher A. Miller
,
Elaine R. Mardis
,
Li Ding
,
and
Richard K. Wilson
Genome Res.
March 2012
22
:
568
-
576
;
Published in Advance
February 2, 2012
,
doi:
10.1101/gr.129684.111
Abstract
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:
PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data
Ken Chen
,
Michael D. McLellan
,
Li Ding
,
Michael C. Wendl
,
Yumi Kasai
,
Richard K. Wilson
,
and
Elaine R. Mardis
Genome Res.
May 2007
17
:
659
-
666
;
Published in Advance
April 6, 2007
,
doi:
10.1101/gr.6151507
Abstract
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:
EAnnot: A genome annotation tool using experimental evidence
Li Ding
,
Aniko Sabo
,
Nicolas Berkowicz
,
Rekha R. Meyer
,
Yoram Shotland
,
Mark R. Johnson
,
Kymberlie H. Pepin
,
Richard K. Wilson
,
and
John Spieth
Genome Res.
December 2004
14
:
2503
-
2509
;
doi:
10.1101/gr.3152604
Abstract
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