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   National Center for Genome Medicine (NCGM), the former National Genotyping Center, was established in 2002.
   NCGM has successfully implemented four platforms for genome research: (1) Short Tandem Repeat Polymorphism (STRP) genotyping platform, (2) Single Nucleotide Polymorphism (SNP) genotyping based on Matrix-Assisted Laser Desorption/Ionization-Time of Flight (MALDI-TOF) mass spectrometry technology, (3) Affymetrix ultra high-throughput SNP genotyping platform (GeneTitan) based on high density oligo-nucleotide hybridization gene chip, (4) illumina MiSeq next generation sequencer. These genome analysis platforms allow this Center to provide various combinations of services according to each investigator’s need.
    In addition to the genotyping and sequencing groups, this Center also has Statistics group and BioIT group. The former is in charge of quality assurance/quality control of genotyping services and perform GWAS analysis; the latter is in charge of developing bioinformatics tools and providing bioinformatics services, such as LIMS, iQuestion, Samportal, GenePipe, HiPipe etc. Notably, by carrying out multiple independent projects, NCGM is proved to be well-integrated and well-qualified to provide a “one stop” service.

Services :

Service Type
Service Code
Service Item
Technology Platform
Sample Management
C2-17
DNA Extraction from 5 mL Whole Blood  
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C2-18
DNA Extraction from 10 mL Whole Blood
C2-19
DNA Storage
C2-26
DNA Extraction from Cultured Cell
SNP Genotyping
C2-7
ENU Mouse Gene Mapping Panel
Sequenom MassARRAY
C2-10
iPLEX SNP Genotyping
C2-12
Mouse Speed Congenics Panel (294 markers & 92 markers)
Whole-Genome SNP Genotyping
C2-15
Axiom Genome-Wide ASI Array Plate
Affymetrix GeneTitan
C2-16
Axiom Genome-Wide CHB Array Plate
C2-42
Axiom Genome-Wide TWB Array Plate
C2-58
Axiom Genome-Wide TWB 2.0 Array Plate
STRP Genotyping
C2-4
PCR Product STRP Genotyping
ABI 3730 DNA Analyzer
Next Generation Sequencing
C2-29
DNA sequencing sample preparation
illumina MiSeq
C2-36
mRNA sequencing sample preparation
C2-37
rRNA-Depleted RNA sequencing sample preparation
C2-43.1
MiSeq Sequencing Service (50 cycles)
C2-43.2
MiSeq Sequencing Service (150 cycles)
C2-43.3
MiSeq Sequencing Service (300 cycles)
C2-43.4
MiSeq Sequencing Service (300 cycles, Micro)
C2-43.5
MiSeq Sequencing Service (300 cycles, Nano)
C2-43.6
MiSeq Sequencing Service (500 cycles)
C2-43.7
MiSeq Sequencing Service (500 cycles, Nano)
C2-43.8
MiSeq Sequencing Service (600 cycles)
C2-48
SureSelect Exome Enrichment (Human/Mouse)
C2-51
DNA library sample preparation by Nextera XT
C2-52.1
MiSeq DNA Library QC (qPCR only)
C2-52.2
MiSeq DNA Library QC (Qubit Fluorometer + Agilent Bioanalyzer HS)
C2-52.3
MiSeq DNA Library QC (Qubit Fluorometer + Agilent Bioanalyzer HS + qPCR)
C2-55.1
RNA QC-Agilent RNA 6000 Nano
C2-55.2
DNA QC-Agilent DNA High Sensitivity
BioIT Services
C2-20
Samportal使用與諮詢
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C2-21
iQuestion使用與諮詢
C2-22
生物資訊分析、軟體開發與諮詢
C2-23
Samportal系統使用費率
C2-24
iQuestion系統使用費率
C2-38
NGS全基因體分析
C2-39
NGS Exome分析
C2-40
NGS RNA分析
C2-49.1
NGS運算分析服務
C2-49.2
NGS資料儲存服務
C2-53
生醫資訊系統使用與諮詢
C2-54
生醫資訊系統使用費率
Statistical Analysis
C2-56
Axiom Array全基因體關聯性分析
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C2-57
資料處理與統計分析
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Customized Service
C2-44
Customized Service
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