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Samantha Zarate

Showing results (1-10 of 9) with videos related to

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Biorxiv : the Preprint Server for Biology|March 3, 2023
Concerning the eXclusion in human genomics: The choice of sex chromosome representation in the human genome drastically affects number of identified variantsBrendan J Pinto, Brian O'Connor, Michael C Schatz, et al.
G3 (Bethesda, Md.)|July 27, 2023
Concerning the eXclusion in human genomics: the choice of sex chromosome representation in the human genome drastically affects the number of identified variantsBrendan J Pinto, Brian O'Connor, Michael C Schatz, et al.
Gigascience|December 21, 2020
Parliament2: Accurate structural variant calling at scaleSamantha Zarate, Andrew Carroll, Medhat Mahmoud, et al.
Genome Biology|December 21, 2021
Hidden biases in germline structural variant detectionMichael M Khayat, Sayed Mohammad Ebrahim Sahraeian, Samantha Zarate, et al.
Nature Communications|September 23, 2020
A diploid assembly-based benchmark for variants in the major histocompatibility complexChen-Shan Chin, Justin Wagner, Qiandong Zeng, et al.
Science (New York, N.Y.)|March 31, 2022
A complete reference genome improves analysis of human genetic variationSergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Cell Genomics|December 1, 2022
Benchmarking challenging small variants with linked and long readsJustin Wagner, Nathan D Olson, Lindsay Harris, et al.
Nature|August 23, 2023
The complete sequence of a human Y chromosomeArang Rhie, Sergey Nurk, Monika Cechova, et al.
Science (New York, N.Y.)|March 31, 2022
The complete sequence of a human genomeSergey Nurk, Sergey Koren, Arang Rhie, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Biorxiv : the Preprint Server for Biology|March 3, 2023
Concerning the eXclusion in human genomics: The choice of sex chromosome representation in the human genome drastically affects number of identified variantsBrendan J Pinto, Brian O'Connor, Michael C Schatz, et al.
G3 (Bethesda, Md.)|July 27, 2023
Concerning the eXclusion in human genomics: the choice of sex chromosome representation in the human genome drastically affects the number of identified variantsBrendan J Pinto, Brian O'Connor, Michael C Schatz, et al.
Gigascience|December 21, 2020
Parliament2: Accurate structural variant calling at scaleSamantha Zarate, Andrew Carroll, Medhat Mahmoud, et al.
Genome Biology|December 21, 2021
Hidden biases in germline structural variant detectionMichael M Khayat, Sayed Mohammad Ebrahim Sahraeian, Samantha Zarate, et al.
Nature Communications|September 23, 2020
A diploid assembly-based benchmark for variants in the major histocompatibility complexChen-Shan Chin, Justin Wagner, Qiandong Zeng, et al.
Science (New York, N.Y.)|March 31, 2022
A complete reference genome improves analysis of human genetic variationSergey Aganezov, Stephanie M Yan, Daniela C Soto, et al.
Cell Genomics|December 1, 2022
Benchmarking challenging small variants with linked and long readsJustin Wagner, Nathan D Olson, Lindsay Harris, et al.
Nature|August 23, 2023
The complete sequence of a human Y chromosomeArang Rhie, Sergey Nurk, Monika Cechova, et al.
Science (New York, N.Y.)|March 31, 2022
The complete sequence of a human genomeSergey Nurk, Sergey Koren, Arang Rhie, et al.
Pageof 1