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Volumn 8, Issue 34, 2017, Pages 56066-56080

Comparative study of whole genome amplification and next generation sequencing performance of single cancer cells

Author keywords

Allelic dropout; CellSave; NGS; SNP; WGA

Indexed keywords

ACCURACY; ANALYTICAL EQUIPMENT; ANALYTICAL PARAMETERS; ARTICLE; BLOOD STORAGE; CANCER CELL; CHEK2 GENE; CLONAL EVOLUTION; CONTROLLED STUDY; COPY NUMBER VARIATION; DNA DETERMINATION; DNA QUALITY; FEASIBILITY STUDY; FGFR2 GENE; GENE; GENE AMPLIFICATION; GENETIC PROCEDURES; GENOMICS; GENOTYPE; HUMAN; HUMAN CELL; INDEL MUTATION; INTERMETHOD COMPARISON; KIT GENE; LIMIT OF DETECTION; MULTIPLE DISPLACEMENT AMPLIFICATION BASED WHOLE GENOME AMPLIFICATION; MULTIPLE DISPLACEMENT AMPLIFICATION POLYMERASE CHAIN REACTION BASED WHOLE GENOME AMPLIFICATION; MUTATIONAL ANALYSIS; NEXT GENERATION SEQUENCING; POLYMERASE CHAIN REACTION BASED WHOLE GENOME AMPLIFICATION; PRAME GENE; SENSITIVITY ANALYSIS; SINGLE CELL ANALYSIS; SINGLE CELL GENOTYPING; SINGLE NUCLEOTIDE POLYMORPHISM; WHOLE EXOME SEQUENCING; WHOLE GENOME AMPLIFICATION;

EID: 85029080506     PISSN: None     EISSN: 19492553     Source Type: Journal    
DOI: 10.18632/oncotarget.10701     Document Type: Article
Times cited : (52)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.