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TAB-Seq
TAB-Seq
Project News:
2014/7/3: EXPERIMENT XML file 'GH265B_L7.2013_03_27.experiment.xml' uploaded
alias: 2013_03_27_ChIP_SR_flowcell-A/fastq_files/lane7.fastq.bz2
expected_number_runs: 1 center_name: UCSD STUDY_REF: The San Diego Epigenome Center SAMPLE_DESCRIPTOR: SRS267133 LIBRARY LIBRARY_NAME: GH265B_L7.2013_03_27 LIBRARY_STRATEGY: TAB-Seq LIBRARY_SOURCE: GENOMIC LIBRARY_SELECTION: RANDOM LIBRARY_LAYOUT: SINGLE POOLING_STRATEGY: none LIBRARY_CONSTRUCTION_PROTOCOL: See http://www.nature.com/nprot/journal/v7/n12/full/nprot.2012.137.html SPOT NUMBER_OF_READS_PER_SPOT: READ_INDEX: 0 READ_CLASS: Application Read READ_TYPE: Forward BASE_COORD: 1 PLATFORM ILLUMINA INSTRUMENT_MODEL: Illumina HiSeq 2500 SEQUENCE_LENGTH: 100 BASE CALLS Illumina HiSeq Control Software 2.0.12.0 QUALITY SCORES Illumina HiSeq Control Software 2.0.12.0 ATTRIBUTES EXPERIMENT_TYPE: DNA Methylation EXTRACTION_PROTOCOL: See http://www.nature.com/nprot/journal/v7/n12/full/nprot.2012.137.html EXTRACTION_PROTOCOL_TYPE_OF_SONICATOR: Covaris EXTRACTION_PROTOCOL_SONICATION_CYCLES: Sonicate the genomic DNA in 120 µl of EB buffer to the desired size range. We typically sonicate for 55 s using a Covaris system, with a 10% duty cycle, intensity set at 4 and cycle per burst set at 200 in order to achieve the size range of 200?500 bp. DNA_PREPARATION_INITIAL_DNA_QNTY: 5ug DNA_PREPARATION_FRAGMENT_SIZE_RANGE: 200-500bp DNA_PREPARATION_ADAPTOR_SEQUENCE: Standard Illumina adaptor sequence DNA_PREPARATION_ADAPTOR_LIGATION_PROTOCOL: TruSeq DNA_PREPARATION_POST-LIGATION_FRAGMENT_SIZE_SELECTION: 250-600 BISULFITE_CONVERSION_PROTOCOL: Convert 450 ng of adapter -ligated DNA as per MethylCode Kit instructions (InvitrogenMECOV-50) BISULFITE_CONVERSION_PERCENT: 99.6405 LIBRARY_GENERATION_PCR_TEMPLATE_CONC: not measured LIBRARY_GENERATION_PCR_POLYMERASE_TYPE: PfuTurbo Cx Hotstart DNA Polymerase, catalog #600410 LIBRARY_GENERATION_PCR_THERMOCYCLING_PROGRAM: 2min 95C, 30s 98C, 10x (15s 98c, 30s 60C, 4min 72C), 10min 72C, hold 4C LIBRARY_GENERATION_PCR_NUMBER_CYCLES: 80 LIBRARY_GENERATION_PCR_F_PRIMER_SEQUENCE: standard Illumina TruSeq LIBRARY_GENERATION_PCR_R_PRIMER_SEQUENCE: standard Illumina TruSeq LIBRARY_GENERATION_PCR_PRIMER_CONC: undiluted Illumina TruSeq kit PCR primers LIBRARY_GENERATION_PCR_PRODUCT_ISOLATION_PROTOCOL: 2% high-resolution (APEX) agarose gel purification. Excise 250-600bp fragment, followed by MinElute-QG purification. |
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