Method for targeted capture of hereditary hearing loss gene sequence and sequencing method

The invention relates to the technical field of biology, and particularly provides a method for targeted capture of a hereditary hearing loss gene sequence and a sequencing method. The method comprises the steps that a capture membrane for targeted capture of positive and negative chains of the here...

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Main Authors JIAO YANG, JIA DANMEI, XU YAPING, CHEN QIONGQIONG, LIU YA, ZHANG JINGLAN, CAI LUHANG, JIA JUNLING
Format Patent
LanguageChinese
English
Published 18.06.2021
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Abstract The invention relates to the technical field of biology, and particularly provides a method for targeted capture of a hereditary hearing loss gene sequence and a sequencing method. The method comprises the steps that a capture membrane for targeted capture of positive and negative chains of the hereditary hearing loss gene exon sequence is prepared, wherein hereditary hearing loss genes comprise CDH23, COL11A1, DSPP, MYO7A, OTOF, PCDH15, MT-RNR1, MT-TL1, MT-TS1, MYO15A, SLC26A4, DFNA5, GJB2, GJB3, KCNJ10, SOX10, TCOF1, WFS1, DFNB59, USH1G, TMC1 and DFNB31; a fragmented human genome sample is constructed into a nucleic acid library applied to high-throughput sequencing; denaturation treatment is conducted on the nucleic acid library, and the nucleic acid library subjected to denaturation treatment is hybridized with the capture membrane under hybridization conditions to form a target nucleic acid molecule-capture membrane compound; and the target nucleic acid molecule-capture membrane compound is cleaned by us
AbstractList The invention relates to the technical field of biology, and particularly provides a method for targeted capture of a hereditary hearing loss gene sequence and a sequencing method. The method comprises the steps that a capture membrane for targeted capture of positive and negative chains of the hereditary hearing loss gene exon sequence is prepared, wherein hereditary hearing loss genes comprise CDH23, COL11A1, DSPP, MYO7A, OTOF, PCDH15, MT-RNR1, MT-TL1, MT-TS1, MYO15A, SLC26A4, DFNA5, GJB2, GJB3, KCNJ10, SOX10, TCOF1, WFS1, DFNB59, USH1G, TMC1 and DFNB31; a fragmented human genome sample is constructed into a nucleic acid library applied to high-throughput sequencing; denaturation treatment is conducted on the nucleic acid library, and the nucleic acid library subjected to denaturation treatment is hybridized with the capture membrane under hybridization conditions to form a target nucleic acid molecule-capture membrane compound; and the target nucleic acid molecule-capture membrane compound is cleaned by us
Author JIA JUNLING
CAI LUHANG
XU YAPING
ZHANG JINGLAN
JIAO YANG
JIA DANMEI
CHEN QIONGQIONG
LIU YA
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– fullname: CAI LUHANG
– fullname: JIA JUNLING
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Snippet The invention relates to the technical field of biology, and particularly provides a method for targeted capture of a hereditary hearing loss gene sequence and...
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SourceType Open Access Repository
SubjectTerms BEER
BIOCHEMISTRY
CHEMISTRY
COMPOSITIONS OR TEST PAPERS THEREFOR
CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL ORENZYMOLOGICAL PROCESSES
ENZYMOLOGY
MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEICACIDS OR MICROORGANISMS
METALLURGY
MICROBIOLOGY
MUTATION OR GENETIC ENGINEERING
PROCESSES OF PREPARING SUCH COMPOSITIONS
SPIRITS
VINEGAR
WINE
Title Method for targeted capture of hereditary hearing loss gene sequence and sequencing method
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