Targeted capture and high-throughput sequencing using molecular inversion probes (MIPs)
Methods in Molecular Biology, ISSN: 1064-3745, Vol: 1492, Page: 95-106
2017
- 17Citations
- 68Captures
- 1Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations17
- Citation Indexes15
- 15
- CrossRef2
- Patent Family Citations2
- Patent Families2
- Captures68
- Readers68
- 68
- Mentions1
- References1
- Wikipedia1
Book Chapter Description
Molecular inversion probes (MIPs) in combination with massively parallel DNA sequencing represent a versatile, yet economical tool for targeted sequencing of genomic DNA. Several thousand genomic targets can be selectively captured using long oligonucleotides containing unique targeting arms and universal linkers. The ability to append sequencing adaptors and sample-specific barcodes allows large-scale pooling and subsequent high-throughput sequencing at relatively low cost per sample. Here, we describe a “wet bench” protocol detailing the capture and subsequent sequencing of >2000 genomic targets from 192 samples, representative of a single lane on the Illumina HiSeq 2000 platform.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84994860454&origin=inward; http://dx.doi.org/10.1007/978-1-4939-6442-0_6; http://www.ncbi.nlm.nih.gov/pubmed/27822858; http://link.springer.com/10.1007/978-1-4939-6442-0_6; https://dx.doi.org/10.1007/978-1-4939-6442-0_6; https://link.springer.com/protocol/10.1007/978-1-4939-6442-0_6
Springer Nature
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