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1 .
A draft human pangenome reference
저자
by
Wen-Wei Liao
;
Mobin Asri
;
Jana Ebler
;
Daniel Doerr
;
Marina Haukness
, et al.
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Nature
. 617:312-324
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7 .
The complete sequence of a human genome
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by
Sergey Nurk
;
Sergey Koren
;
Arang Rhie
;
Mikko Rautiainen
;
Andrey V. Bzikadze
, et al.
소스
Science (New York, N.Y.), vol 376, iss 6588
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7 .
Chasing perfection: validation and polishing strategies for telomere-to-telomere genome assemblies
저자
by
Alaina Shumate
;
Jonathan Wood
;
Benedict Paten
;
Karen H. Miga
;
Giulio Formenti
, et al.
소스
Nature Methods
. 19:687-695
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7 .
Accelerated identification of disease-causing variants with ultra-rapid nanopore genome sequencing
저자
by
Sneha D. Goenka
;
John E. Gorzynski
;
Kishwar Shafin
;
Dianna G. Fisk
;
Trevor Pesout
, et al.
소스
Nature Biotechnology
. 40:1035-1041
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7 .
Best: A Tool for Characterizing Sequencing Errors
저자
by
Daniel Liu
;
Anastasiya Belyaeva
;
Kishwar Shafin
;
Pi-Chuan Chang
;
Andrew Carroll
, et al.
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7 .
The complete sequence of a human Y chromosome
저자
by
Arang Rhie
;
Sergey Nurk
;
Monika Cechova
;
Savannah J. Hoyt
;
Dylan J. Taylor
, et al.
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7 .
Benchmarking challenging small variants with linked and long reads
저자
by
Justin Wagner
;
Nathan D. Olson
;
Lindsay Harris
;
Ziad Khan
;
Jesse Farek
, et al.
소스
Cell genomics
. 2(5)
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7 .
DeepConsensus improves the accuracy of sequences with a gap-aware sequence transformer
저자
by
Gunjan Baid
;
Daniel E. Cook
;
Kishwar Shafin
;
Taedong Yun
;
Felipe Llinares-López
, et al.
소스
Nature Biotechnology
.
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7 .
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions
저자
by
Nathan D. Olson
;
Justin Wagner
;
Jennifer McDaniel
;
Sarah H. Stephens
;
Samuel T. Westreich
, et al.
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Cell genomics
. 2(5)
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7 .
Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting
저자
by
John E. Gorzynski
;
Sneha D. Goenka
;
Kishwar Shafin
;
Tanner D. Jensen
;
Dianna G. Fisk
, et al.
소스
New England Journal of Medicine
. 386:700-702
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