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mapping 250k sty2 snp array  (Thermo Fisher)


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    Structured Review

    Thermo Fisher mapping 250k sty2 snp array
    Gli2 has higher expression than Gli1 in DDLPS tumors but not as a result of Gli1 amplification. Gli1 and Gli2 mRNA expressions were evaluated in two separate cohorts (TCGA-SARC n = 58) ( A ) and <t>GSE21124</t> ( n = 50) of DDLPS tumors ( B ). Gli1 mRNA expression was compared to Gli1 genomic status in the respective cohorts ( C , D ), as was Gli2 mRNA expression ( E , F ). Pearson correlation analysis was performed to evaluate the strength of the relationship between Gli1 and Gli2 expression in DDLPS tumors in both cohorts ( G , H ). Statistical evaluation was performed following Rout’s outlier test with subsequent Student’s t -test or one-way ANOVA when appropriate. Outliers were removed as follows: 3B, Gli1 n = 6; 3C, Diploid n = 7, Gain n = 2, Amp. n = 1; 3D, Diploid, n = 1. Paired values from patient tumors were removed following outlier removal. (ns: not significant, ** p < 0.01, *** p < 0.001, **** p < 0.0001).
    Mapping 250k Sty2 Snp Array, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "Bioinformatics Screen Reveals Gli-Mediated Hedgehog Signaling as an Associated Pathway to Poor Immune Infiltration of Dedifferentiated Liposarcoma"

    Article Title: Bioinformatics Screen Reveals Gli-Mediated Hedgehog Signaling as an Associated Pathway to Poor Immune Infiltration of Dedifferentiated Liposarcoma

    Journal: Cancers

    doi: 10.3390/cancers15133360

    Gli2 has higher expression than Gli1 in DDLPS tumors but not as a result of Gli1 amplification. Gli1 and Gli2 mRNA expressions were evaluated in two separate cohorts (TCGA-SARC n = 58) ( A ) and GSE21124 ( n = 50) of DDLPS tumors ( B ). Gli1 mRNA expression was compared to Gli1 genomic status in the respective cohorts ( C , D ), as was Gli2 mRNA expression ( E , F ). Pearson correlation analysis was performed to evaluate the strength of the relationship between Gli1 and Gli2 expression in DDLPS tumors in both cohorts ( G , H ). Statistical evaluation was performed following Rout’s outlier test with subsequent Student’s t -test or one-way ANOVA when appropriate. Outliers were removed as follows: 3B, Gli1 n = 6; 3C, Diploid n = 7, Gain n = 2, Amp. n = 1; 3D, Diploid, n = 1. Paired values from patient tumors were removed following outlier removal. (ns: not significant, ** p < 0.01, *** p < 0.001, **** p < 0.0001).
    Figure Legend Snippet: Gli2 has higher expression than Gli1 in DDLPS tumors but not as a result of Gli1 amplification. Gli1 and Gli2 mRNA expressions were evaluated in two separate cohorts (TCGA-SARC n = 58) ( A ) and GSE21124 ( n = 50) of DDLPS tumors ( B ). Gli1 mRNA expression was compared to Gli1 genomic status in the respective cohorts ( C , D ), as was Gli2 mRNA expression ( E , F ). Pearson correlation analysis was performed to evaluate the strength of the relationship between Gli1 and Gli2 expression in DDLPS tumors in both cohorts ( G , H ). Statistical evaluation was performed following Rout’s outlier test with subsequent Student’s t -test or one-way ANOVA when appropriate. Outliers were removed as follows: 3B, Gli1 n = 6; 3C, Diploid n = 7, Gain n = 2, Amp. n = 1; 3D, Diploid, n = 1. Paired values from patient tumors were removed following outlier removal. (ns: not significant, ** p < 0.01, *** p < 0.001, **** p < 0.0001).

    Techniques Used: Expressing, Amplification

    Datasets used and accession locations.
    Figure Legend Snippet: Datasets used and accession locations.

    Techniques Used: Expressing, Cell Differentiation, Sequencing, RNA Sequencing Assay

    Related Articles

    other:

    Article Title: The nuclear deubiquitinase BAP1 is commonly inactivated by somatic mutations and 3p21.1 losses in malignant pleural mesothelioma
    Article Snippet: DNAs from cell lines were hybridized to Affymetrix 250K SNP arrays according to the manufacturer’s instructions.

    Article Title: Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutation.
    Article Snippet: Congenital myopathies describe a group of inherited muscle disorders with neonatal or infantile onset typically associated with muscle weakness, respiratory involvement and delayed motor milestones.. We previously reported a novel congenital myopathy in an inbred Samaritan family.. All patients displayed severe neonatal hypotonia and respiratory distress, and unlike other congenital myopathies, a constantly improving health status.

    Article Title: Biallelic Mutations in the Autophagy Regulator DRAM2 Cause Retinal Dystrophy with Early Macular Involvement
    Article Snippet: Homozygosity mapping was performed with Affymetrix 250K SNP arrays on genomic DNA from seven affected individuals from family ES1.

    Article Title: Recent genetic discoveries in osteoporosis, sarcopenia and obesity [Review]
    Article Snippet: In 2014, we reported a large-scale association study for low lean body mass using Affymetrix 250K SNP arrays in Japanese postmenopausal women [93].

    Article Title: The architecture and evolution of cancer neochromosomes.
    Article Snippet: The 778 and 449 neochromosomes were analyzed using Affymetrix 250k SNP arrays (Figure 1D).

    Software:

    Article Title: Fructose 1,6-bisphosphatase deficiency: enzyme and mutation analysis performed on calcitriol-stimulated monocytes with a note on long-term prognosis.
    Article Snippet: Fructose 1,6-bisphosphatase (FBPase) deficiency is an inborn error of metabolism in the gluconeogenetic pathway.. During periods of low food intake or infections, a defect in FBPase can result in hypoglycemia, ketonuria and metabolic acidosis.. We established a diagnostic system for FBPase deficiency consisting of enzyme activity measurement and mutation detection in calcitriol-stimulated monocytes.

    Extraction:

    Article Title: Fructose 1,6-bisphosphatase deficiency: enzyme and mutation analysis performed on calcitriol-stimulated monocytes with a note on long-term prognosis.
    Article Snippet: Fructose 1,6-bisphosphatase (FBPase) deficiency is an inborn error of metabolism in the gluconeogenetic pathway.. During periods of low food intake or infections, a defect in FBPase can result in hypoglycemia, ketonuria and metabolic acidosis.. We established a diagnostic system for FBPase deficiency consisting of enzyme activity measurement and mutation detection in calcitriol-stimulated monocytes.

    Multiple Displacement Amplification:

    Article Title: Mosaic Copy Number Variation in Human Neurons
    Article Snippet: .. After multiple displacement amplification (MDA) ( 14 ), we hybridized single hiPSC-derived neuronal genomes to Affymetrix 250K SNP arrays (as in ( 11 )). .. We subjected single neurons from post-mortem tissue to Illumina DNA sequencing using a custom version of the single cell sequencing protocol developed by Navin et al. ( 12 ), which combines the GenomePlex whole-genome amplification method with Nextera-based library preparation ( 15 ).

    Genome Wide:

    Article Title: Identification of two novel PNPLA1 mutations in Turkish families with autosomal recessive congenital ichthyosis.
    Article Snippet: .. Affymetrix 250K SNP arrays were used in order to perform genome-wide analysis according to manufacturer’s recommendations. ..



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    Gli2 has higher expression than Gli1 in DDLPS tumors but not as a result of Gli1 amplification. Gli1 and Gli2 mRNA expressions were evaluated in two separate cohorts (TCGA-SARC n = 58) ( A ) and <t>GSE21124</t> ( n = 50) of DDLPS tumors ( B ). Gli1 mRNA expression was compared to Gli1 genomic status in the respective cohorts ( C , D ), as was Gli2 mRNA expression ( E , F ). Pearson correlation analysis was performed to evaluate the strength of the relationship between Gli1 and Gli2 expression in DDLPS tumors in both cohorts ( G , H ). Statistical evaluation was performed following Rout’s outlier test with subsequent Student’s t -test or one-way ANOVA when appropriate. Outliers were removed as follows: 3B, Gli1 n = 6; 3C, Diploid n = 7, Gain n = 2, Amp. n = 1; 3D, Diploid, n = 1. Paired values from patient tumors were removed following outlier removal. (ns: not significant, ** p < 0.01, *** p < 0.001, **** p < 0.0001).
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    Gli2 has higher expression than Gli1 in DDLPS tumors but not as a result of Gli1 amplification. Gli1 and Gli2 mRNA expressions were evaluated in two separate cohorts (TCGA-SARC n = 58) ( A ) and <t>GSE21124</t> ( n = 50) of DDLPS tumors ( B ). Gli1 mRNA expression was compared to Gli1 genomic status in the respective cohorts ( C , D ), as was Gli2 mRNA expression ( E , F ). Pearson correlation analysis was performed to evaluate the strength of the relationship between Gli1 and Gli2 expression in DDLPS tumors in both cohorts ( G , H ). Statistical evaluation was performed following Rout’s outlier test with subsequent Student’s t -test or one-way ANOVA when appropriate. Outliers were removed as follows: 3B, Gli1 n = 6; 3C, Diploid n = 7, Gain n = 2, Amp. n = 1; 3D, Diploid, n = 1. Paired values from patient tumors were removed following outlier removal. (ns: not significant, ** p < 0.01, *** p < 0.001, **** p < 0.0001).
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    Comparison of RegBounder to MCR and leave-1-out procedures applied to primary lung adenocarcinomas . The advantages of RegBounder over previous peak-finding procedures are illustrated for two well-described oncogene peaks identified in GISTIC analysis of 371 lung adenocarcinoma samples characterized on the Affymetrix <t>250K</t> <t>StyI</t> <t>SNP</t> array (as published in ). (a) A well-described amplification peak is identified on chromosome 12p12.1 with MCR (red dotted lines) near to but not containing the known lung cancer oncogene KRAS . Because there are more than two apparent passenger events in this region, the leave-1-out peak (blue dotted lines) also does not contain KRAS . However, RegBounder (green dotted lines) produces a wider peak that captures KRAS . (b) An amplification peak on chromosome 5p15.33 contains hTERT , the catalytic subunit of the human telomerase holoenzyme, within the MCR (red dotted lines). In this case, RegBounder (green dotted lines) produces a narrower peak region than the corresponding leave-1-out peak (blue dotted lines), demonstrating the ability of RegBounder to achieve a greater balance between peak region size and accuracy. In both (a) and (b), the y-axis depicts the amplification G-score and the x-axis denotes position along the corresponding chromosome.
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    Image Search Results


    Gli2 has higher expression than Gli1 in DDLPS tumors but not as a result of Gli1 amplification. Gli1 and Gli2 mRNA expressions were evaluated in two separate cohorts (TCGA-SARC n = 58) ( A ) and GSE21124 ( n = 50) of DDLPS tumors ( B ). Gli1 mRNA expression was compared to Gli1 genomic status in the respective cohorts ( C , D ), as was Gli2 mRNA expression ( E , F ). Pearson correlation analysis was performed to evaluate the strength of the relationship between Gli1 and Gli2 expression in DDLPS tumors in both cohorts ( G , H ). Statistical evaluation was performed following Rout’s outlier test with subsequent Student’s t -test or one-way ANOVA when appropriate. Outliers were removed as follows: 3B, Gli1 n = 6; 3C, Diploid n = 7, Gain n = 2, Amp. n = 1; 3D, Diploid, n = 1. Paired values from patient tumors were removed following outlier removal. (ns: not significant, ** p < 0.01, *** p < 0.001, **** p < 0.0001).

    Journal: Cancers

    Article Title: Bioinformatics Screen Reveals Gli-Mediated Hedgehog Signaling as an Associated Pathway to Poor Immune Infiltration of Dedifferentiated Liposarcoma

    doi: 10.3390/cancers15133360

    Figure Lengend Snippet: Gli2 has higher expression than Gli1 in DDLPS tumors but not as a result of Gli1 amplification. Gli1 and Gli2 mRNA expressions were evaluated in two separate cohorts (TCGA-SARC n = 58) ( A ) and GSE21124 ( n = 50) of DDLPS tumors ( B ). Gli1 mRNA expression was compared to Gli1 genomic status in the respective cohorts ( C , D ), as was Gli2 mRNA expression ( E , F ). Pearson correlation analysis was performed to evaluate the strength of the relationship between Gli1 and Gli2 expression in DDLPS tumors in both cohorts ( G , H ). Statistical evaluation was performed following Rout’s outlier test with subsequent Student’s t -test or one-way ANOVA when appropriate. Outliers were removed as follows: 3B, Gli1 n = 6; 3C, Diploid n = 7, Gain n = 2, Amp. n = 1; 3D, Diploid, n = 1. Paired values from patient tumors were removed following outlier removal. (ns: not significant, ** p < 0.01, *** p < 0.001, **** p < 0.0001).

    Article Snippet: Genomics array profiling was collected using the Affymetrix Mapping 250K Sty2 SNP Array (GSE21124 [ ]).

    Techniques: Expressing, Amplification

    Datasets used and accession locations.

    Journal: Cancers

    Article Title: Bioinformatics Screen Reveals Gli-Mediated Hedgehog Signaling as an Associated Pathway to Poor Immune Infiltration of Dedifferentiated Liposarcoma

    doi: 10.3390/cancers15133360

    Figure Lengend Snippet: Datasets used and accession locations.

    Article Snippet: Genomics array profiling was collected using the Affymetrix Mapping 250K Sty2 SNP Array (GSE21124 [ ]).

    Techniques: Expressing, Cell Differentiation, Sequencing, RNA Sequencing Assay

    Comparison of RegBounder to MCR and leave-1-out procedures applied to primary lung adenocarcinomas . The advantages of RegBounder over previous peak-finding procedures are illustrated for two well-described oncogene peaks identified in GISTIC analysis of 371 lung adenocarcinoma samples characterized on the Affymetrix 250K StyI SNP array (as published in ). (a) A well-described amplification peak is identified on chromosome 12p12.1 with MCR (red dotted lines) near to but not containing the known lung cancer oncogene KRAS . Because there are more than two apparent passenger events in this region, the leave-1-out peak (blue dotted lines) also does not contain KRAS . However, RegBounder (green dotted lines) produces a wider peak that captures KRAS . (b) An amplification peak on chromosome 5p15.33 contains hTERT , the catalytic subunit of the human telomerase holoenzyme, within the MCR (red dotted lines). In this case, RegBounder (green dotted lines) produces a narrower peak region than the corresponding leave-1-out peak (blue dotted lines), demonstrating the ability of RegBounder to achieve a greater balance between peak region size and accuracy. In both (a) and (b), the y-axis depicts the amplification G-score and the x-axis denotes position along the corresponding chromosome.

    Journal: Genome Biology

    Article Title: GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers

    doi: 10.1186/gb-2011-12-4-r41

    Figure Lengend Snippet: Comparison of RegBounder to MCR and leave-1-out procedures applied to primary lung adenocarcinomas . The advantages of RegBounder over previous peak-finding procedures are illustrated for two well-described oncogene peaks identified in GISTIC analysis of 371 lung adenocarcinoma samples characterized on the Affymetrix 250K StyI SNP array (as published in ). (a) A well-described amplification peak is identified on chromosome 12p12.1 with MCR (red dotted lines) near to but not containing the known lung cancer oncogene KRAS . Because there are more than two apparent passenger events in this region, the leave-1-out peak (blue dotted lines) also does not contain KRAS . However, RegBounder (green dotted lines) produces a wider peak that captures KRAS . (b) An amplification peak on chromosome 5p15.33 contains hTERT , the catalytic subunit of the human telomerase holoenzyme, within the MCR (red dotted lines). In this case, RegBounder (green dotted lines) produces a narrower peak region than the corresponding leave-1-out peak (blue dotted lines), demonstrating the ability of RegBounder to achieve a greater balance between peak region size and accuracy. In both (a) and (b), the y-axis depicts the amplification G-score and the x-axis denotes position along the corresponding chromosome.

    Article Snippet: We made use of a large collection of 3,131 cancer samples run on the Affymetrix 250K StyI SNP Array [ ] plus several hundred additional samples run on the Affymetrix SNP6.0 Array (data not shown).

    Techniques: Amplification