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microarray data files  (Pathwork Diagnostics Inc)

 
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    Pathwork Diagnostics Inc microarray data files
    Microarray Data Files, supplied by Pathwork Diagnostics Inc, 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/microarray+files/microarray+data+files/pmc03614454-168-1-7
    Average 90 stars, based on 1 article reviews
    microarray data files - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Validation and Reproducibility of a Microarray-Based Gene Expression Test for Tumor Identification in Formalin-Fixed, Paraffin-Embedded Specimens
    Article Snippet: The microarray data file (CEL) is then transmitted to Pathwork Diagnostics ... Tissue calls issued by the test for 462 evaluable specimens were compared with the known diagnoses for the specimens.

    Microarray:

    Article Title: A gene expression profile test to resolve head & neck squamous versus lung squamous cancers
    Article Snippet: .. All microarray data files were transferred to Pathwork Diagnostics for data quality assessment and analysis through GEP-HN-LS. ..

    Article Title: Interlaboratory Performance of a Microarray-Based Gene Expression Test to Determine Tissue of Origin in Poorly Differentiated and Undifferentiated Cancers
    Article Snippet: .. The resulting microarray data files were sent electronically in blinded manner to Pathwork Diagnostics for processing and generation of scores for each TOO type. ..



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    Likely pathogenic CNVs found in the cohort.

    Journal: Scientific Reports

    Article Title: A cohort study of neurodevelopmental disorders and/or congenital anomalies using high resolution chromosomal microarrays in southern Brazil highlighting the significance of ASD

    doi: 10.1038/s41598-024-54385-2

    Figure Lengend Snippet: Likely pathogenic CNVs found in the cohort.

    Article Snippet: We collected a total of 1120 chromosomal microarray (CMA) read files that were performed by the Laboratório Neurogene in Florianópolis, Santa Catarina, Brazil, upon request by medical geneticists and neurologists for investigative/diagnostic purposes, primarily from the Joana de Gusmão Children's Hospital, but also from MDs from the University Hospital Professor Polydoro Ernani de São Thiago and from private clinics in Florianópolis, State of Santa Catarina, between 2013 and 2019.

    Techniques: Microarray

    Cases with potential UPDs, where a single autosomal chromosome presented LCSH(s) over 3 Mbp, that that alone or in addition of LCSHs ≥ 3 Mbp reached a size of ≥ 10 Mbp with no other LSCH over 5 Mbp on any other autosomal chromosome.

    Journal: Scientific Reports

    Article Title: A cohort study of neurodevelopmental disorders and/or congenital anomalies using high resolution chromosomal microarrays in southern Brazil highlighting the significance of ASD

    doi: 10.1038/s41598-024-54385-2

    Figure Lengend Snippet: Cases with potential UPDs, where a single autosomal chromosome presented LCSH(s) over 3 Mbp, that that alone or in addition of LCSHs ≥ 3 Mbp reached a size of ≥ 10 Mbp with no other LSCH over 5 Mbp on any other autosomal chromosome.

    Article Snippet: We collected a total of 1120 chromosomal microarray (CMA) read files that were performed by the Laboratório Neurogene in Florianópolis, Santa Catarina, Brazil, upon request by medical geneticists and neurologists for investigative/diagnostic purposes, primarily from the Joana de Gusmão Children's Hospital, but also from MDs from the University Hospital Professor Polydoro Ernani de São Thiago and from private clinics in Florianópolis, State of Santa Catarina, between 2013 and 2019.

    Techniques: Reflux, Microarray