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Emerging technologies for prenatal diagnosis: The application of whole genome and RNA sequencing.
Prenat Diagn. 2022 May;42(6):686-696. doi: 10.1002/pd.6146. Epub 2022 Apr 18.
Prenat Diagn. 2022.
PMID: 35416301
Free PMC article.
Review.
Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits.
Yuan B, Schulze KV, Assia Batzir N, Sinson J, Dai H, Zhu W, Bocanegra F, Fong CT, Holder J, Nguyen J, Schaaf CP, Yang Y, Bi W, Eng C, Shaw C, Lupski JR, Liu P.
Yuan B, et al.
Genome Med. 2022 Sep 30;14(1):113. doi: 10.1186/s13073-022-01113-y.
Genome Med. 2022.
PMID: 36180924
Free PMC article.
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The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation.
Du H, Jolly A, Grochowski CM, Yuan B, Dawood M, Jhangiani SN, Li H, Muzny D, Fatih JM, Coban-Akdemir Z, Carlin ME, Scheuerle AE, Witzl K, Posey JE, Pendleton M, Harrington E, Juul S, Hastings PJ, Bi W, Gibbs RA, Sedlazeck FJ, Lupski JR, Carvalho CMB, Liu P.
Du H, et al.
Genome Med. 2022 Oct 27;14(1):122. doi: 10.1186/s13073-022-01123-w.
Genome Med. 2022.
PMID: 36303224
Free PMC article.
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