Results 251 to 260 of about 574,833 (290)

Community Assembly Processes of Deadwood Mycobiome in a Tropical Forest Revealed by Long-Read Third-Generation Sequencing. [PDF]

Microb Ecol
Purahong W, Ji L, Wu YT.
europepmc   +1 more source

Thalassemia screening by third-generation sequencing: Pilot study in a Thai population. [PDF]

Obstet Med
Traisrisilp K, Zheng Y, Choy KW, Chareonkwan P.   +3 more
europepmc   +1 more source

Molecular characterization of similar Hb Lepore Boston-Washington in four Chinese families using third generation sequencing. [PDF]

Sci Rep
Zhuang J, Zhang N, Zheng Y, Jiang Y, Chen Y, Mao A, Chen C.   +6 more
europepmc   +1 more source

Third-generation sequencing identified two rare α-chain variants leading to hemoglobin variants in Chinese population. [PDF]

Mol Genet Genomic Med
Zhuang J, Jiang Y, Chen Y, Mao A, Chen J, Chen C.   +5 more
europepmc   +1 more source

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Third-generation sequencing for genetic disease

Clinica Chimica Acta, 2023
Third-generation sequencing (TGS) has led to a brave new revolution in detecting genetic diseases over the last few years. TGS has been rapidly developed for genetic disease applications owing to its significant advantages such as long read length, rapid detection, and precise detection of complex and rare structural variants.
Xiaoting Ling, Chenghan Wang, Linlin Li, Liqiu Pan, Chaoyu Huang, Caixia Zhang, Yunhua Huang, Yuling Qiu, Faquan Lin, Yifang Huang   +9 more
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Quality of Third Generation Sequencing

Journal of Computational and Theoretical Nanoscience, 2020
Third generation sequencing (TGS) relates to long reads but with relatively high error rates. Quality of TGS is a hot topic, dealing with errors. This paper combines and investigates three quality related metrics. They are basecalling accuracy, Phred Quality Scores, and GC content. For basecalling accuracy, a deep neural network is adopted.
Ali Elbialy, M. A. El-Dosuky, Ibrahim M. El-Henawy   +2 more
openaire   +1 more source

Full-Length Transcript Phasing with Third-Generation Sequencing

2022
Haplotyping individual full-length transcripts can be important in diagnosis and treatment of certain genetic diseases. One set of diseases, repeat expansions 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 ...
Nenad, Svrzikapa, Ramakrishna, Boyanapalli   +1 more
openaire   +2 more sources