The largest database of trusted experimental protocols

Infinium human cytosnp 850k v1.2 beadchip

Manufactured by Illumina
Sourced in United States

The Infinium Human CytoSNP-850K v1.2 BeadChip is a high-density genotyping array designed for comprehensive cytogenetic analysis. It features over 850,000 genetic markers across the human genome, enabling the detection of chromosomal abnormalities and copy number variations.

Automatically generated - may contain errors

2 protocols using infinium human cytosnp 850k v1.2 beadchip

1

Genomic Copy Number Profiling of Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
Genomic DNA of unedited and edited clones of THP-1 and Jurkat cell lines, and patient-derived LCLs was used for SNP-array copy number profiling and analysis of regions of homozygosity with the Infinium Human CytoSNP-850K v1.2 BeadChip (Illumina, San Diego, CA, USA). This array has ∼850,000 single nucleotide polymorphisms (SNPs) markers across the genome and can detect genomic insertions and deletions as well as stretches of homozygosity. Data analysis was conducted using NxClinical software v6.0 (Bionano genomics, San Diego, CA, USA). Human genome build Feb. 2009 GRCh37/hg19 was used. Results were classified with BENCH Lab CNV software (Agilent, Santa Clara, CA, USA). The genotype data were used for cell line verification and monitoring for potential genomic alterations in single cell cultures.
+ Open protocol
+ Expand
2

SNP-Array Copy Number Profiling of CRISPR-Edited LCLs

Check if the same lab product or an alternative is used in the 5 most similar protocols
SNP-array copy number profiling and analysis of regions of homozygosity were performed on DNA isolated from WT and CRISPR-Cas9 edited LCLs (ERAP2-KO) according to standard procedures using the Infinium Human CytoSNP-850K v1.2 BeadChip (Illumina, San Diego, CA, USA). Samples were scanned using the iScan system (Illumina). Subsequently, visualizations of SNP-array results and data analysis were carried out using NxClinical software v5.1 (BioDiscovery, Los Angeles, CA, USA). Human genome build Feb. 2009 GRCh37/hg19 was used.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!