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Titlebook: Haplotyping; Methods and Protocol Brock A. Peters,Radoje Drmanac Book 2023 The Editor(s) (if applicable) and The Author(s), under exclusive

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41#
發(fā)表于 2025-3-28 14:36:06 | 只看該作者
Youtao Liu,Fei Fan,Radoje Drmanac,Brock A. Peters,Ou Wangngineering, energy production and storage, sensors, medicine, nanotechnology, military and aerospace, oil and gas recovery, thermal insulation and household uses are being developed with an estimated annual market growth rate of around 70% until 2015.The Aerogels Handbook summarizes state-of-the-art
42#
發(fā)表于 2025-3-28 19:10:56 | 只看該作者
43#
發(fā)表于 2025-3-29 00:55:23 | 只看該作者
44#
發(fā)表于 2025-3-29 04:44:25 | 只看該作者
45#
發(fā)表于 2025-3-29 10:18:33 | 只看該作者
Margret R. Hoehe,Ralf Herwigients and possible in-flight emergencies and their appropriated treatment.?.Containing several new chapters and featuring extensively updated contributions from experts in the field, ?Aeromedical Evacuation: Ma978-3-030-15905-4978-3-030-15903-0
46#
發(fā)表于 2025-3-29 13:27:19 | 只看該作者
47#
發(fā)表于 2025-3-29 19:02:23 | 只看該作者
Targeted Locus Amplification and Haplotyping, As TLA is based on proximity ligation, variants can be linked to each other, thereby enabling allelic phasing and the generation of haplotypes. This allows for the study of genetic variants in an allele-specific manner. Here, we provide a step-by-step protocol for TLA sample preparation and a compl
48#
發(fā)表于 2025-3-29 22:17:06 | 只看該作者
Full-Length Transcript Phasing with Third-Generation Sequencing,pansions of simple tandem repeat sequences are the cause of over 40 neurological disorders. In many of these conditions, expanding a polymorphic repeat beyond a given threshold has been strongly associated with disease onset and severity. Given that most repeat expansions are inherited in an autosom
49#
發(fā)表于 2025-3-30 00:26:32 | 只看該作者
50#
發(fā)表于 2025-3-30 06:48:16 | 只看該作者
Low-Cost Genome-Scale Phasing with Barcode-Linked Sequencing,and which feature both accurate base calling and long-range DNA phasing capability. The NGS revolution has struggled to meet the latter of these needs. Here we describe a protocol to address this limitation by preserving the molecular origin of short sequencing reads with an insignificant increase t
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