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4×180k wholegenome oligonucleotide microarray  (WholeGenome LLC)

 
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    WholeGenome LLC 4×180k wholegenome oligonucleotide microarray
    4×180k Wholegenome Oligonucleotide Microarray, supplied by WholeGenome LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/180k+oligonucleotide+microarray/4%C3%97180k+wholegenome+oligonucleotide+microarray/pm36849228-44-23-24
    Average 90 stars, based on 1 article reviews
    4×180k wholegenome oligonucleotide microarray - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Sequencing:

    Article Title: TRAPPC2L-related disorder: first homozygous protein-truncating variant and further delineation of the phenotype.
    Article Snippet: .. Array CGH and intellectual disability (ID) gene panel sequencing Patient IV- 3 was first analysed with routine comparative genomic hybridisation (CGH) testing using 4×180K wholegenome oligonucleotide microarray and SureSelect XT Inherited Diseases Panel sequencing (Agilent Technologies, Santa Clara, California, USA) following the manufacturer’s protocol. .. Whole- exome sequencing of proband IV- 3, his father (III- 7) and a healthy brother (IV- 2) (figure 1A) was performed using the SeqCap EZ MedExome sequencing kit (Roche NimbleGen, Basel, Switzerland) following standard protocols.

    Hybridization:

    Article Title: TRAPPC2L-related disorder: first homozygous protein-truncating variant and further delineation of the phenotype.
    Article Snippet: .. Array CGH and intellectual disability (ID) gene panel sequencing Patient IV- 3 was first analysed with routine comparative genomic hybridisation (CGH) testing using 4×180K wholegenome oligonucleotide microarray and SureSelect XT Inherited Diseases Panel sequencing (Agilent Technologies, Santa Clara, California, USA) following the manufacturer’s protocol. .. Whole- exome sequencing of proband IV- 3, his father (III- 7) and a healthy brother (IV- 2) (figure 1A) was performed using the SeqCap EZ MedExome sequencing kit (Roche NimbleGen, Basel, Switzerland) following standard protocols.

    Microarray:

    Article Title: TRAPPC2L-related disorder: first homozygous protein-truncating variant and further delineation of the phenotype.
    Article Snippet: .. Array CGH and intellectual disability (ID) gene panel sequencing Patient IV- 3 was first analysed with routine comparative genomic hybridisation (CGH) testing using 4×180K wholegenome oligonucleotide microarray and SureSelect XT Inherited Diseases Panel sequencing (Agilent Technologies, Santa Clara, California, USA) following the manufacturer’s protocol. .. Whole- exome sequencing of proband IV- 3, his father (III- 7) and a healthy brother (IV- 2) (figure 1A) was performed using the SeqCap EZ MedExome sequencing kit (Roche NimbleGen, Basel, Switzerland) following standard protocols.



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    Copy number status and fragment orientation as revealed by chromosomal microarray (CMA) and whole genome sequencing (WGS) of the complex rearrangements.

    Journal: PLoS Genetics

    Article Title: Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization

    doi: 10.1371/journal.pgen.1007780

    Figure Lengend Snippet: Copy number status and fragment orientation as revealed by chromosomal microarray (CMA) and whole genome sequencing (WGS) of the complex rearrangements.

    Article Snippet: In 13 cases (P2046_133, P2109_123, P2109_150, P2109_151, P2109_162, P2109_188, P2109_190, P2109_302, P4855_511, P4855_512, P2109_176, P1426_301, P2109_185), the CMA was performed with an 180K custom oligonucleotide microarray with whole genome coverage and a median resolution of approximately 18 kb (Oxford Gene Technology (OGT), Oxfordshire, UK).

    Techniques: Microarray, Sequencing