Assess the risk probability of the gene knockout in 1 second. This system is developed based on 30 million CRISPR library screening data covering 1400+ cell types. Precisely identify essential genes, ensure the safety of experiments.
Found the gene of interest barely expresses in the wild-type cell line when the KO experiment was almost completed? This system, based on the RNA-seq data from 1400+ cells, grades the expression level according to the TPM value, making gene-editing valuable.
What if you find the target gene would not induce lethal but it’s still hard to get the KO homozygotes, the reason is that the karyotype of the target cell line is too complex, with a high copy number! This system, based on genome sequencing results of 1000 cells, can intelligently calculate the copy number of the gene of interest, and helps you select the suitable cell line to easily get KO homozygotes!
Pool Phase: Analyze the gene-editing efficiency, and intelligently determine different genotypes and their proportions. Single-cell clone Phase: High throughput reading of gene sequencing results, automated analysis of clone genotypes. Help you clearly identify the positive clones!
Help you analyze gene sequencing data. Upload Sanger sequencing file and input the theoretical sequence to compare the two and evaluate your sequencing results.
Automatically design primers to validate the targeting site
Analyze the total GC content and distribution of a sequence
Convert a DNA sequence into its reverse, complementary, or reverse complementary sequence
Translate DNA sequence into protein sequence
Find out the repeat, reverse and similar complementary fragments between the two sequences.
Find out the common region and differences between the two sequences.