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Whole genome shotgun bisulfite sequencing of the IMR90 cell line
Whole genome shotgun bisulfite sequencing of the IMR90 cell line
Project News:
2009/7/21: EXPERIMENT XML file 'ecker.methylC-seq_imr90_r2c.experiment.xml' uploaded
alias: methylC-seq_imr90_r2c
expected_number_runs: 3 expected_number_spots: 5000000000 expected_number_reads: 2500000000 center_name: UCSD STUDY_REF: The San Diego Epigenome Center SAMPLE_DESCRIPTOR: IMR90_r2 LIBRARY LIBRARY_NAME: methylC-seq_imr90_r2c LIBRARY_STRATEGY: Bisulfite-Seq LIBRARY_SOURCE: GENOMIC LIBRARY_SELECTION: RANDOM LIBRARY_LAYOUT: SINGLE LIBRARY_CONSTRUCTION_PROTOCOL: Genomic DNA was purified from IMR90 human embryonic stem cells, sheared by sonication to 50-500 bp, ligated to methylated single-end Illumina adaptors, fragments of 140-210 bp isolated after agarose gel electrophoresis, bisulfite converted, amplified by PCR and sequenced using the Illumina Genome Analyzer II according to manufacturer's instructions SPOT SPOT_DECODE_METHOD: 0 PLATFORM ILLUMINA INSTRUMENT_MODEL: Illumina Genome Analyzer II CYCLE_SEQUENCE: normal CYCLE_COUNT: 87 BASE CALLS SEQUENCE_SPACE: Base Space BASE_CALLER: Bustard QUALITY SCORES Quality Type: phred QUALITY_SCORER: Bustard NUMBER_OF_LEVELS: 1 MULTIPLIER: 1 ATTRIBUTES EXPERIMENT_TYPE: DNA Methylation EXTRACTION_PROTOCOL: Qiagen DNeasy mini kit, performed as per manufacturer's instructions' EXTRACTION_PROTOCOL_TYPE_OF_SONICATOR: Diagenode Bioruptor EXTRACTION_PROTOCOL_SONICATION_CYCLES: 20 cycles of: 30 seconds on high power, 2 minutes off DNA_PREPARATION_INITIAL_DNA_QNTY: 5 µg DNA_PREPARATION_FRAGMENT_SIZE_RANGE: 50-500 bp DNA_PREPARATION_ADAPTOR_SEQUENCE: A: 5' P-GATCGGAAGAGCTCGTATGCCGTCTTCTGCTTG, B: 5' ACACTCTTTCCCTACACGACGCTCTTCCGATCT DNA_PREPARATION_ADAPTOR_LIGATION_PROTOCOL: Standard Illumina genomic DNA library preparation ligation protocol (15 minutes at room temperature), except the adapters contained methylcytosine and were supplied by Illumina DNA_PREPARATION_POST-LIGATION_FRAGMENT_SIZE_SELECTION: Separation by electrophoresis on a 2% agarose gel followed by excision of 140-210 bp fragments BISULFITE_CONVERSION_PROTOCOL: Standard Human Genetic Signatures MethylEasy Xceed bisulfite conversion kit protocol BISULFITE_CONVERSION_PERCENT: 99.6% of cytosines converted based on shotgun sequencing of unmethylated lambda phage control spiked into original genomic DNA sample LIBRARY_GENERATION_PCR_TEMPLATE_CONC: One third of the 140-210 nt adapter-ligated, bisulfite converted DNA was used in each 50 µl PCR reaction LIBRARY_GENERATION_PCR_POLYMERASE_TYPE: Stratagene Pfu Turbo Cx LIBRARY_GENERATION_PCR_THERMOCYCLING_PROGRAM: 95?C 2 min; 98?C 30 sec, 4 cycles of 98?C 15 sec, 60?C 30 sec, 72?C 4 min; 72?C 10 min LIBRARY_GENERATION_PCR_NUMBER_CYCLES: 4 LIBRARY_GENERATION_PCR_F_PRIMER_SEQUENCE: 5' AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT LIBRARY_GENERATION_PCR_R_PRIMER_SEQUENCE: 5' CAAGCAGAAGACGGCATACGAGCTCTTCCGATCT LIBRARY_GENERATION_PCR_PRIMER_CONC: 25 µM LIBRARY_GENERATION_PCR_PRODUCT_ISOLATION_PROTOCOL: Separation by electrophoresis on a 2% agarose gel followed by excision of 180-300 bp fragments. |
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