Zobrazeno 1 - 10
of 48 237
pro vyhledávání: '"read"'
Autor:
LE GOFF, DELPHINE, WYBO, GILLES
Publikováno v:
Stratégies. 10/12/2023, Issue 2190, p8-12. 4p.
Autor:
PIERCE, DENNIS
Publikováno v:
Library Journal. Aug2023, Vol. 148 Issue 8, p34-40. 7p. 1 Color Photograph.
Autor:
Read, Sally
Publikováno v:
Logos: A Journal of Catholic Thought & Culture. Summer2024, Vol. 27 Issue 3, p135-136. 2p.
Autor:
Herbst, John W.
Publikováno v:
Catholic Biblical Quarterly. Oct2024, Vol. 86 Issue 4, p820-821. 3p.
Autor:
Knapp, Maggie
Publikováno v:
Library Journal. Oct2024, Vol. 149 Issue 10, p126-126. 1/5p. 1 Color Photograph.
Autor:
Ferreira, Kelly
Publikováno v:
Booklist. 2/15/2023, Vol. 119 Issue 12, p71-82. 12p.
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract Copy number variants (CNVs) are structural variants within the eukaryotic genome that vary among individuals of a species. These variants have been associated with different phenotypic traits, making them a valuable consideration as markers
Externí odkaz:
https://doaj.org/article/a8a3ee0dc0294589b6e5666b603c1be5
Autor:
Banks, Thomas
Publikováno v:
New Oxford Review. Sep2024, Vol. 91 Issue 7, p42-44. 3p.
Autor:
Ahuvia, Mika
Publikováno v:
Catholic Biblical Quarterly. Jul2024, Vol. 86 Issue 3, p608-610. 3p.
Autor:
Liang Zong, Yabing Zhu, Yuan Jiang, Ying Xia, Qun Liu, Jing Wang, Song Gao, Bei Luo, Yongxian Yuan, Jingjiao Zhou, Sanjie Jiang
Publikováno v:
RNA Biology, Vol 21, Iss 1, Pp 122-131 (2024)
Next-generation sequencing has revolutionized cancer genomics by enabling high-throughput mutation screening yet detecting fusion genes reliably remains challenging. Long-read sequencing offers potential for accurate fusion transcript identification,
Externí odkaz:
https://doaj.org/article/d7f4ce570d1d4f228c960017df1f4f18