DVID
|
5002307 |
VISID
|
TVIS20004218
|
Chromosome
|
chr13 |
GRCh38 Location
|
73513425 |
Disease
|
Cervical carcinoma |
Sample
|
Cell line |
Virus Reference Genome
|
Not given |
Literature Information
PubMed PMID
|
30679491
|
Published year
|
2019 |
Journal
|
Scientific reports |
Title
|
TaME-seq: An efficient sequencing approach for characterisation of HPV genomic variability and chromosomal integration. |
Author
|
Lagström S,Umu SU,Lepistö M,Ellonen P,Meisal R,Christiansen IK,Ambur OH,Rounge TB |
Evidence
|
HPV genomic variability and chromosomal integration are important in the HPV-induced carcinogenic process. TaME-seq combines tagmentation and multiplex PCR enrichment for simultaneous analysis of HPV variation and chromosomal integration, and it can also be adapted to other viruses. Chromosomal integration breakpoints and large deletions were identified in HPV positive cell lines and in one clinical sample. Efficient identification of both HPV variability and integration sites will be important for the study of HPV evolution and adaptability and may be an important tool for use in cervical cancer diagnostics.
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