Nature, Год журнала: 2022, Номер 607(7917), С. 176 - 184
Опубликована: Май 20, 2022
Язык: Английский
Nature, Год журнала: 2022, Номер 607(7917), С. 176 - 184
Опубликована: Май 20, 2022
Язык: Английский
Nature Genetics, Год журнала: 2019, Номер 51(12), С. 1664 - 1669
Опубликована: Ноя. 29, 2019
Язык: Английский
Процитировано
880Nature, Год журнала: 2019, Номер 573(7772), С. 45 - 54
Опубликована: Авг. 28, 2019
Язык: Английский
Процитировано
628Nature Reviews Genetics, Год журнала: 2019, Номер 21(2), С. 71 - 87
Опубликована: Окт. 11, 2019
Язык: Английский
Процитировано
604Journal of Genetic Engineering and Biotechnology, Год журнала: 2021, Номер 19(1), С. 128 - 128
Опубликована: Авг. 27, 2021
DNA markers improved the productivity and accuracy of classical plant breeding by means marker-assisted selection (MAS). The enormous number quantitative trait loci (QTLs) mapping read for different species have given a plenitude molecular marker-gene associations. In this review, we discussed positive aspects its precise applications in programmes. Molecular has considerably shortened time new crop varieties to be brought market. To explore information about markers, many reviews been published last few decades; all these were intended breeders obtain on genetics. synopsis recent developments their application programmes devoted early with little or no knowledge markers. progress made breeding, genetics, genomics selection, editing genome contributed comprehensive understanding provides several proofs genetic diversity available plants greatly complemented devices. MAS revolutionized process acceleration accuracy, which is continuously empowering around world.
Язык: Английский
Процитировано
342Nature, Год журнала: 2022, Номер 604(7905), С. 310 - 315
Опубликована: Апрель 6, 2022
Abstract Comprehensive genome annotation is essential to understand the impact of clinically relevant variants. However, absence a standard for clinical reporting and browser display complicates process consistent interpretation reporting. To address these challenges, Ensembl/GENCODE 1 RefSeq 2 launched joint initiative, Matched Annotation from NCBI EMBL-EBI (MANE) collaboration, converge on human gene transcript jointly define high-value set transcripts corresponding proteins. Here, we describe MANE sets use as universal standards variant display. The Select identifies representative each protein-coding gene, whereas Plus Clinical provides additional at loci where alone are not sufficient report all currently known Each represents an exact match between exonic sequences its counterpart in such that identifiers can be used synonymously. We have now released 97% genes, including American College Medical Genetics Genomics Secondary Findings list v3.0 (ref. 3 ) genes. accessible major browsers key resources. Widespread adoption will increase consistency reporting, facilitate exchange data regardless source help streamline interpretation.
Язык: Английский
Процитировано
341Nature Reviews Molecular Cell Biology, Год журнала: 2021, Номер 22(12), С. 815 - 833
Опубликована: Авг. 16, 2021
Язык: Английский
Процитировано
338Nature Cell Biology, Год журнала: 2019, Номер 21(10), С. 1286 - 1299
Опубликована: Сен. 30, 2019
Язык: Английский
Процитировано
297Nature Reviews Molecular Cell Biology, Год журнала: 2019, Номер 20(12), С. 766 - 784
Опубликована: Сен. 26, 2019
Язык: Английский
Процитировано
268Science China Life Sciences, Год журнала: 2020, Номер 63(7), С. 953 - 985
Опубликована: Апрель 30, 2020
Язык: Английский
Процитировано
264Nature Reviews Genetics, Год журнала: 2020, Номер 22(4), С. 235 - 250
Опубликована: Ноя. 26, 2020
Язык: Английский
Процитировано
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