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- 文献和实验
- 技术资料
- 保存条件:
Freezer (-20 o C)
- 保质期:
详询
- 英文名:
Human DNA for Whole-Genome Variant Assessment (Daughter of Utah/European Ancestry) (HG-001)
- 库存:
20
- 供应商:
南京北鱼生物科技有限公司
- CAS号:
n/a
- 规格:
1 vial

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文献和实验[1] Zook, J.M.; McDaniel, J; Olsen, N.D.; Wagner, J.; Parikh, H.; Heaton, H.; Irvine, S.A.; Trigg, L.; Truty, R.;
McLean, C.Y.; De La Vega, F.M.; Xiao, C.; Sherry, S.; Salit, M.; An Open Resource for Accurately
Benchmarking Small Variant and Reference Calls; Nat. Biotech., Vol. 37, pp. 561-566 (2019
Genome‐Scale Sequencing to Identify Genes Involved in Mendelian Disorders
variant. The fact that each parent's pair of variants is cis‐oriented is known because there are short reads with both variants, and short reads with neither variant. The affected sibling has DNA variations on both alleles, in contrast
genome. Nature 409:860‐921. Langmead, B., Trapnell, C., Pop, M., and Salzberg, S.L. 2009. Ultrafast and memory‐efficient alignment of short DNA sequences to the human genome
【共享】某机构发表的核酸相关研究的文章(EST,SNP等),PDF全文下载
, ..., Rosenthal A, ..., Platzer M, Shimizu N, Lander ES (2006) DNA sequence and analysis of human chromosome 8 Nature 436: 331-335 pdf Platzer M (2006) The human genome and its upcoming dynamics In Genome Dynamics. vol. 2. Volff, J-N, ed. Pp. 1-16. Basel: S
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