A high frequency of sequence alterations is due to formalin fixation of archival specimens.
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Identification of high-confidence somatic mutations in whole genome sequence of formalin-fixed breast cancer specimensIn vitro mutation artifacts after formalin fixation and error prone translesion synthesis during PCRPrevalence of von Hippel-Lindau gene mutations in sporadic renal cell carcinoma: results from The Netherlands cohort studyAnalysis of Pre-Analytic Factors Affecting the Success of Clinical Next-Generation Sequencing of Solid Organ MalignanciesNext-generation sequencing to guide cancer therapyMolecular testing guideline for selection of lung cancer patients for EGFR and ALK tyrosine kinase inhibitors: guideline from the College of American Pathologists, International Association for the Study of Lung Cancer, and Association for MolecularComprehensive genomic studies: emerging regulatory, strategic, and quality assurance challenges for biorepositoriesVHL mutations and their correlation with tumour cell proliferation, microvessel density, and patient prognosis in clear cell renal cell carcinoma.Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine.The pseudo-mitochondrial genome influences mistakes in heteroplasmy interpretationK-Ras mutation detection in liquid biopsy and tumor tissue as prognostic biomarker in patients with pancreatic cancer: a systematic review with meta-analysis.The impact of tissue fixatives on morphology and antibody-based protein profiling in tissues and cells.Targeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation.Detection of somatic mutations in tumors using unaligned clonal sequencing data.A retrospective immunohistochemical study reveals atypical scrapie has existed in the United Kingdom since at least 1987.High-resolution comparative genomic hybridization detects extra chromosome arm 12p material in most cases of carcinoma in situ adjacent to overt germ cell tumors, but not before the invasive tumor development.Spatio-temporal changes in the structure of an Australian frog hybrid zone: a 40-year perspective.Improved resolution by mounting of tissue sections for laser microdissection.CD117+ small cell lung cancer lacks the asp 816-->val point mutation in exon 17.RCL2, a new fixative, preserves morphology and nucleic acid integrity in paraffin-embedded breast carcinoma and microdissected breast tumor cells.Manual versus laser micro-dissection in molecular biology.A high throughput combinatorial library technique for identifying formalin-sensitive epitopesA candidate precursor to serous carcinoma that originates in the distal fallopian tube.Detection of pre-invasive lung cancer: technical aspects of the LIFE project.Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD).High resolution melting analysis for rapid and sensitive EGFR and KRAS mutation detection in formalin fixed paraffin embedded biopsies.DNA damage in preserved specimens and tissue samples: a molecular assessment.Mutation detection by real-time PCR: a simple, robust and highly selective method.Differentiated vulvar intraepithelial neoplasia contains Tp53 mutations and is genetically linked to vulvar squamous cell carcinoma.Detection of BRCA1 and BRCA2 Ashkenazi Jewish founder mutations in formalin-fixed paraffin-embedded tissues using conventional PCR and heteroduplex/amplicon size differencesKRAS analysis in colorectal carcinoma: analytical aspects of Pyrosequencing and allele-specific PCR in clinical practiceDetection of somatic mutations by high-resolution DNA melting (HRM) analysis in multiple cancers.Systematic comparison of two whole-genome amplification methods for targeted next-generation sequencing using frozen and FFPE normal and cancer tissues.Exploiting formalin-preserved fish specimens for resources of DNA barcoding.The role of replicates for error mitigation in next-generation sequencing.KRAS mutation testing in the treatment of metastatic colorectal cancer with anti-EGFR therapies.EGFR and KRAS mutation analysis in cytologic samples of lung adenocarcinoma enabled by laser capture microdissection.KRAS genotyping in rectal adenocarcinoma specimens with low tumor cellularity after neoadjuvant treatment.Discrepancies between VEGF -1154 G>A polymorphism analysis performed in peripheral blood samples and FFPE tissueMolecular testing guideline for selection of lung cancer patients for EGFR and ALK tyrosine kinase inhibitors: guideline from the College of American Pathologists, International Association for the Study of Lung Cancer, and Association for Molecular
P2860
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P2860
A high frequency of sequence alterations is due to formalin fixation of archival specimens.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
A high frequency of sequence a ...... ixation of archival specimens.
@en
type
label
A high frequency of sequence a ...... ixation of archival specimens.
@en
prefLabel
A high frequency of sequence a ...... ixation of archival specimens.
@en
P2093
P2860
P1476
A high frequency of sequence a ...... ixation of archival specimens.
@en
P2093
Lundeberg J
Söderkvist P
Williams C
P2860
P304
P356
10.1016/S0002-9440(10)65461-2
P407
P577
1999-11-01T00:00:00Z