ID
45251
Descrizione
Principal Investigator: Haig H. Kazazian, Jr, MD, University of Pennsylvania School of Medicine, Philadelphia, PA, USA MeSH: Normalcy https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000273 The aim of this study is to discover LINE-1 (L1) insertion sites present in humans that are absent from the reference genome sequence. We use the distinguishing nucleotide characteristics of human-specific L1 elements to resequence the L1 3' flanking regions thus locating the L1 insertion sites whether or not they are present in the reference genome assembly. In doing so, we have uncovered a higher than expected number of non-reference L1 insertions, an average of 152 insertions per individual. In addition, we find that any two individuals differ at an average of 285 sites with respect to presence or absence of L1 insertions in those sites, and use this to estimate the rate of retrotransposition in humans at 1 event per 140 live births (95% c.i. 1/95 to 1/270). We show that individual 'L1 profiles' recapitulate genetic ancestry as expected, and find that dimorphic insertions are more frequent in introns relative to fixed insertions.
collegamento
Keywords
versioni (2)
- 04/07/22 04/07/22 - Chiara Middel
- 12/10/22 12/10/22 - Adrian Schulz
Titolare del copyright
Haig H. Kazazian, Jr, MD, University of Pennsylvania School of Medicine, Philadelphia, PA, USA
Caricato su
12 ottobre 2022
DOI
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Licenza
Creative Commons BY 4.0
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dbGaP phs000273 High-Throughput Retrotransposon Discovery in Humans
This data table contains a listing of subjects, subject consent groups, and mapping of subject IDs to the subject IDs of the source repository (Spinner, Toda and Yolken labs and Coriell).
- StudyEvent: SEV1
- This data table contains a listing of subjects, subject consent groups, and mapping of subject IDs to the subject IDs of the source repository (Spinner, Toda and Yolken labs and Coriell).
- This data table contains pedigree, gender, and twin information of study participants.
- The data table contains mapping of study subject IDs to sample IDs, and sample IDs to sample IDs of the source repository (Spinner, Toda and Yolken labs and Coriell).
Similar models
This data table contains a listing of subjects, subject consent groups, and mapping of subject IDs to the subject IDs of the source repository (Spinner, Toda and Yolken labs and Coriell).
- StudyEvent: SEV1
- This data table contains a listing of subjects, subject consent groups, and mapping of subject IDs to the subject IDs of the source repository (Spinner, Toda and Yolken labs and Coriell).
- This data table contains pedigree, gender, and twin information of study participants.
- The data table contains mapping of study subject IDs to sample IDs, and sample IDs to sample IDs of the source repository (Spinner, Toda and Yolken labs and Coriell).
C3847505 (UMLS CUI [1,2])
C0449416 (UMLS CUI [1,2])
C3847505 (UMLS CUI [1,3])