Sequencing XMET genes to promote genotype-guided risk assessment and precision medicine-Reference-Cited by-同舟云学术

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Sequencing XMET genes to promote genotype-guided risk assessment and precision medicine

Published:2019-05-20 Issue:7 Volume:62 Page:895-904
ISSN:1674-7305
Container-title:Science China Life Sciences
language:en
Short-container-title:Sci. China Life Sci.

Author:

Jin Yaqiong,Chen Geng,Xiao Wenming,Hong Huixiao,Xu Joshua,Guo Yongli,Xiao Wenzhong,Shi Tieliu,Shi Leming,Tong Weida,Ning Baitang

Publisher

Springer Science and Business Media LLC

Subject

General Agricultural and Biological Sciences,General Environmental Science,General Biochemistry, Genetics and Molecular Biology

Link

http://link.springer.com/content/pdf/10.1007/s11427-018-9479-5.pdf

Reference99 articles.

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2. Abyzov, A., and Gerstein, M. (2011). AGE: defining breakpoints of genomic structural variants at single-nucleotide resolution, through optimal alignments with gap excision. Bioinformatics 27, 595–603.

3. Abyzov, A., Urban, A.E., Snyder, M., and Gerstein, M. (2011). CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. Genome Res 21, 974–984.

4. Alkan, C., Kidd, J.M., Marques-Bonet, T., Aksay, G., Antonacci, F., Hormozdiari, F., Kitzman, J.O., Baker, C., Malig, M., Mutlu, O., et al. (2009). Personalized copy number and segmental duplication maps using next-generation sequencing. Nat Genet 41, 1061–1067.

5. Ambardar, S., and Gowda, M. (2018). High-resolution full-length HLA typing method using third generation (Pac-Bio SMRT) sequencing technology. Methods Mol Biol 1802, 135–153.

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