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Sample GSM1493416 Query DataSets for GSM1493416
Status Public on May 15, 2015
Title S2_ebv12_picoplex
Sample type genomic
 
Source name EBV-transformed lymphoblast
Organism Homo sapiens
Characteristics cell type: EBV-transformed lymphoblast
dna sample: Single cell
wga: PicoPlex
hybridization protocol: Conventional
Treatment protocol Cultured cells were washed with phosphate buffered saline (PBS) solution to completely remove medium traces prior to the single cell isolation.
Growth protocol EBV-transformed lymphoblastoid cells were cultured in 75-cm2 plastic flasks (BD Falcon, USA) in Dulbecco's Modified Eagle Medium/Nutrient Mixture F-12 (DMEM/F12) (Gibco, USA) medium supplemented with 10% Fetal Bovine Serum (FBS) (Thermo Scientific, USA) at 37oC, 5% CO2.
Extracted molecule genomic DNA
Extraction protocol Single-cell DNA was amplified following: (i) an MDA approach with Genomi Phi V2 (GE Healthcare, Piscataway, NJ). Single cells were washed in 1xPBS and transferred into a 200 µl PCR tube containing 1.5 µl alkaline lysis buffer (ALB; 200 mM KOH and 50 mM DTT) by mouth controlled pipetting using 75 µm stripper tips (Origio, Denmark). The samples were stored at -20°C for at least 30 min and were further incubated for 10 min at 65°C prior to the multiple displacement amplification (MDA) reaction. Single cell DNA was amplified following an MDA-approach with GenomiPhiV2 (GE Healthcare, USA). The MDA products were purified using the High Pure PCR Product Purification Kit (Roche, Switzerland) and resuspended in 70 µl of elution buffer. All amplification products were quantified with a spectrophotometer (Nanodrop ND-1000 spectrophotometer). Single-cell amplifications yielding less than 2 µg DNA were not further used. (ii) A PCR-based approach with PicoPlex (Rubicon Genomics, MI, USA). Single cells were washed in 1xPBS and transferred into a 200 µl PCR tube containing 1.5 µl PBS by mouth controlled pipetting using 75 µm stripper tips (Origio, Denmark). The samples were further whole genome amplified using PicoPLEX (Rubicon Genomics, USA), according to the protocol of the manufacturer. The WGA products were purified using the High Pure PCR Product Purification Kit (Roche, Switzerland) and resuspended in 70 µl of elution buffer. All amplification products were quantified with a spectrophotometer (Nanodrop ND-1000 spectrophotometer; Nanodrop Technologies). Single-cell amplifications yielding less than 2 µg DNA were not further used.
Label biotin
Label protocol according to Affymetrix GeneChip Mapping 500K Assay Manual
 
Hybridization protocol according to Affymetrix GeneChip Mapping 500K Assay Manual
Scan protocol according to Affymetrix GeneChip Mapping 500K Assay Manual
Description Single cell from an Epstein-Barr virus transformed lymphoblastoid cell line derived from sibling S2.
Data processing All the DNA samples were genotyped using the dynamic model (DM) algorithm embedded in the ‘GeneChip Genotyping Analysis Software (GTYPE) version 4.1 (Affymetrix)’ using a homozygous and heterozygous calling threshold of 0.12, (2) the BRLMM algorithm within the ‘Genotyping console 3.0.1’ software (Affymetrix) using a scoring threshold of 0.1 and (3) the Birdseed algorithm using both 'birdseed-v1' and 'birdseed-dev' versions. The latter is the most recently incorporated development version of birdseed from The Broad Institute (http://www.broadinstitute.org/mpg/birdsuite/birdseed.html).
The CEL files are provided online, and DM-determined genotypes are provided in the 'NspMatrix' sheet.
 
Submission date Aug 28, 2014
Last update date May 16, 2015
Contact name Masoud Zamani Esteki
E-mail(s) [email protected]
Phone +31 43 38 75306
Organization name Maastricht University Medical Center
Department Clinical Genetics
Lab Cellular Genomic Medicine
Street address P. Debyelaan 25
City Maastricht
State/province Limburg
ZIP/Postal code 6229 HX
Country Netherlands
 
Platform ID GPL3718
Series (2)
GSE60907 Concurrent whole-genome haplotyping and copy number profiling of single cells (Affymetrix)
GSE60910 Concurrent whole-genome haplotyping and copy number profiling of single cells

Data table header descriptions
ID_REF
VALUE genotype call

Data table
ID_REF VALUE
SNP_A-1780520 No Call
SNP_A-1780618 No Call
SNP_A-1780632 AA
SNP_A-1780654 No Call
SNP_A-4192495 AB
SNP_A-4192498 No Call
SNP_A-1780732 No Call
SNP_A-1780848 No Call
SNP_A-1780985 No Call
SNP_A-1781022 No Call
SNP_A-1781076 No Call
SNP_A-1781249 No Call
SNP_A-1781276 BB
SNP_A-1781302 No Call
SNP_A-1781510 BB
SNP_A-4192564 No Call
SNP_A-1781614 No Call
SNP_A-1781633 No Call
SNP_A-1781764 BB
SNP_A-1781829 No Call

Total number of rows: 262264

Table truncated, full table size 5348 Kbytes.




Supplementary file Size Download File type/resource
GSM1493416_Sample_11.CEL.gz 21.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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