{"database":"biostudies-arrayexpress","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown","Transcriptomics","Genomics","Proteomics"],"submitter":["Hagit Philip"],"instrument_platform":["Illumina MiSeq"],"study_type":["genotyping by high throughput sequencing"],"organism":["Homo sapiens"],"species":["Homo sapiens"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/E-MTAB-13682"],"description":["Haploid human embryonic stem cells harboring TP53 or MLH1 knockout (KO) were subjected to a genome-wide CRISPR-Cas9 knockout screen to identify synthetic lethal interactions associated with the mentioned genes."],"repository":["biostudies-arrayexpress"],"sample_protocol":["Sequencing - MiSeq illumina","Library Construction - prepare mix inside a PCR hood, after cleaning the surface with DNase Away and70% EtOH. If possible, we recommend setting up at least 4 parallel PCRs for a given sample.Final contents of each reaction:• 10 μL 10x reaction buffer• 8 μL dNTP• 0.5 μL P5 primer mix, 100 μM• 1.5 μL ExTaq polymerase• up to 10 μg of genomic DNA or 200 ng of plasmid DNA• 10 μL of P7 primer 5 μM• up to 100 μL with water1. Make a master mix of reaction buffer, dNTP, P5 primer mix, taq polymerase, and water.Aliquot into a PCR plate.2. Add template DNA.3. Add a unique P7 primer to barcode each individual reaction.Thermal cycler parametersWait for block to reach 95°C before adding samples.1. 95°C, 1 minute2. 95°C 30 seconds (denaturation)3. 53°C 30 seconds (annealing)4. 72°C 30 seconds (extension)Back to step 2, total of 28 cycles5. 72°C 10 minutes6. 4°C forever","Sample Collection - Wash cells with PBS x2. Trypsinize (TrypLE Select) the wells with the regular protocol. Spin down the cells after neutralizing the trypsin with a serum-containing medium. Count cellsfreeze pellet","Nucleic Acid Extraction - gSYNC DNA Extraction Kit (GS100)"],"figure_sub":["Organization","MINSEQE Score","Assays and Data","MAGE-TAB Files"],"pubmed_authors":["Hagit Philip"],"additional_accession":[]},"is_claimable":false,"name":"Genome-wide KO CRISPR-Cas9 screen on Haploid human embryonic stem cells with TP53 or MLH1 LoF","description":"Haploid human embryonic stem cells harboring TP53 or MLH1 knockout (KO) were subjected to a genome-wide CRISPR-Cas9 knockout screen to identify synthetic lethal interactions associated with the mentioned genes.","dates":{"release":"2025-12-14T00:00:00Z","modification":"2025-12-14T02:02:16.522Z","creation":"2024-01-02T17:03:05.209Z"},"accession":"E-MTAB-13682","cross_references":{"ENA":["ERP156422"],"Biostudies":["E-MTAB-13685","E-MTAB-13683","E-MTAB-13684"],"EFO":["EFO_0002944","EFO_0004170","EFO_0002771","EFO_0005518","EFO_0004184"]}}