Detalhe da pesquisa
1.
A new approach to decode DNA methylome and genomic variants simultaneously from double strand bisulfite sequencing.
Brief Bioinform
; 22(6)2021 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-34058751
2.
MFEprimer-3.0: quality control for PCR primers.
Nucleic Acids Res
; 47(W1): W610-W613, 2019 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31066442
3.
CirGRDB: a database for the genome-wide deciphering circadian genes and regulators.
Nucleic Acids Res
; 46(D1): D64-D70, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29059379
4.
Genetic landscape of papillary thyroid carcinoma in the Chinese population.
J Pathol
; 244(2): 215-226, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29144541
5.
TET1 modulates H4K16 acetylation by controlling auto-acetylation of hMOF to affect gene regulation and DNA repair function.
Nucleic Acids Res
; 45(2): 672-684, 2017 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-27733505
6.
Population Genomics Reveals Speciation and Introgression between Brown Norway Rats and Their Sibling Species.
Mol Biol Evol
; 34(9): 2214-2228, 2017 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28482038
7.
RBP-Var: a database of functional variants involved in regulation mediated by RNA-binding proteins.
Nucleic Acids Res
; 44(D1): D154-63, 2016 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26635394
8.
Dysplastic spondylolysis is caused by mutations in the diastrophic dysplasia sulfate transporter gene.
Proc Natl Acad Sci U S A
; 112(26): 8064-9, 2015 Jun 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-26077908
9.
Lysosomal storage disease in the brain: mutations of the ß-mannosidase gene identified in autosomal dominant nystagmus.
Genet Med
; 17(12): 971-9, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25741867
10.
A Bayesian framework to identify methylcytosines from high-throughput bisulfite sequencing data.
PLoS Comput Biol
; 10(9): e1003853, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25255082
11.
Androgen deprivation drives variation of androgen receptor trinucleotide repeats.
Acta Biochim Biophys Sin (Shanghai)
; 51(9): 972-975, 2019 Sep 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31392319
12.
Extend the benchmarking indel set by manual review using the individual cell line sequencing data from the Sequencing Quality Control 2 (SEQC2) project.
Sci Rep
; 14(1): 7028, 2024 03 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38528062
13.
Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility.
Hum Mutat
; 33(12): 1635-8, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22865819
14.
Gnas Promoter Hypermethylation in the Basolateral Amygdala Regulates Reconsolidation of Morphine Reward Memory in Rats.
Genes (Basel)
; 13(3)2022 03 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35328106
15.
Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions.
Genome Biol
; 22(1): 109, 2021 04 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-33863344
16.
Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families.
Biochem Biophys Res Commun
; 399(4): 647-53, 2010 Sep 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-20691156
17.
Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation.
Mol Genet Metab
; 101(2-3): 192-9, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20728388
18.
Inter- and intratumor DNA methylation heterogeneity associated with lymph node metastasis and prognosis of esophageal squamous cell carcinoma.
Theranostics
; 10(7): 3035-3048, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32194853
19.
Screening for possible oligogenic pathogenesis in Chinese sporadic ALS patients.
Amyotroph Lateral Scler Frontotemporal Degener
; 19(5-6): 419-425, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29411640
20.
Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing.
J Genet Genomics
; 45(10): 527-538, 2018 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-30392784