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发帖数: 1972 | 1 Recent advances in whole-genome sequencing have brought the vision of
personal genomics and genomic medicine
closer to reality. However, current methods lack clinical accuracy and the
ability to describe the context (haplotypes) in
which genome variants co-occur in a cost-effective manner. Here we describe
a low-cost DNA sequencing and
haplotyping process, long fragment read (LFR) technology, which is similar
to sequencing long single DNA molecules
without cloning or separation of metaphase chro... 阅读全帖 |
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