Clinical Next Generation Sequencing Leveraging Unique Molecular Barcodes in Somatic Mutation Calling Absent a Matched-Normal

Bigdeli A.; Ganapathy K.; Sussman R.; Morrisette J. D.; Faryabi R. B.

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Clinical Next Generation Sequencing Leveraging Unique Molecular Barcodes in Somatic Mutation Calling Absent a Matched-Normal

机译：临床下一代测序利用各种分子条形码在体细胞突变呼叫中缺乏匹配正常

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《The Journal of molecular diagnostics: JMD》 |2017年第6期|共1页
作者
Bigdeli A.; Ganapathy K.; Sussman R.; Morrisette J. D.; Faryabi R. B.;
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Hosp Univ Penn 3400 Spruce St Philadelphia PA 19104 USA;

Hosp Univ Penn 3400 Spruce St Philadelphia PA 19104 USA;

Hosp Univ Penn 3400 Spruce St Philadelphia PA 19104 USA;

Univ Penn Philadelphia PA 19104 USA;

Univ Penn Philadelphia PA 19104 USA;

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正文语种 eng
中图分类临床医学;
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1. Clinical Next Generation Sequencing Leveraging Unique Molecular Barcodes in Somatic Mutation Calling Absent a Matched-Normal [J] . Bigdeli A., Ganapathy K., Sussman R., The Journal of molecular diagnostics: JMD . 2017,第6期

机译：临床下一代测序利用各种分子条形码在体细胞突变呼叫中缺乏匹配正常
2. Accuracy and reproducibility of somatic point mutation calling in clinical-type targeted sequencing data [J] . Ali Karimnezhad, Gareth A. Palidwor, Kednapa Thavorn, BMC Medical Genomics . 2020,第1期

机译：临床型靶向测序数据中躯体点突变的准确性和再现性
3. A Singularity Container for Molecular Diagnostic Somatic Variant Calling on the Ion Torrent Next-Generation Sequencing Platform [J] . Andrea Garofoli, Viola Paradiso, Hesam Montazeri, The Journal of molecular diagnostics: JMD . 2019,第5期

机译：一种奇异性容器，用于对离子洪流下一代测序平台进行离子诊断躯体变体的奇异容器
4. PAS-MUT with Somatic Mutations in Cancer and Classified Diseases for Clinical-Genomics Research: PAS-MUT Somatic Mutations [C] . Saman Zeeshan, Zeeshan Ahmed IEEE International Conference on Bioinformatics and Biomedicine . 2019

机译：具有癌症和分类疾病中的体细胞突变的PAS-MUT用于临床基因组学研究：PAS-MUT和体细胞突变
5. Computational assessment of somatic missense mutations detected in tumor sequencing studies with cancer-specific high-throughput annotation of somatic mutations (CHASM). [D] . Carter, Hannah. 2012

机译：具有肿瘤特异性高通量体细胞突变（CHASM）的肿瘤测序研究中检测到的体细胞错义突变的计算评估。
6. Selective identification of somatic mutations in pancreatic cancer cells through a combination of next-generation sequencing of plasma DNA using molecular barcodes and a bioinformatic variant filter [O] . Yoji Kukita, Kazuyoshi Ohkawa, Ryoji Takada, 2012

机译：通过使用分子条形码和生物信息学变体过滤器的下一代血浆DNA测序的组合，选择性鉴定胰腺癌细胞中的体细胞突变
7. Accuracy and reproducibility of somatic point mutation calling in clinical-type targeted sequencing data [O] . Ali Karimnezhad, Gareth A. Palidwor, Kednapa Thavorn, 2020

机译：临床型靶向测序数据中躯体点突变的准确性和再现性

Clinical Next Generation Sequencing Leveraging Unique Molecular Barcodes in Somatic Mutation Calling Absent a Matched-Normal

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