deseq2 module of partek flow genomic analysis software (Partek)
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Partek
deseq2 module of partek flow genomic analysis software
Deseq2 Module Of Partek Flow Genomic Analysis Software, supplied by Partek, 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/deseq2+module+of+partek+flow+genomic+analysis+software/deseq2/pm38281697-76-5-8
Average 90 stars, based on 1 article reviews
Deseq2 Module Of Partek Flow Genomic Analysis Software, supplied by Partek, 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/deseq2+module+of+partek+flow+genomic+analysis+software/deseq2/pm38281697-76-5-8
Average 90 stars, based on 1 article reviews
deseq2 module of partek flow genomic analysis software - by Bioz Stars,
2026-10
90/100 stars
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Gene Expression:Article Title: DNMT1 Y495C mutation interferes with maintenance methylation of imprinting control regions. Article Snippet: Hereditary Sensory and Autonomic Neuropathy Type 1E (HSAN1E) is a rare autosomal dominant neurological disorder due to missense mutations in DNA methyltransferase 1 (DNMT1).. To investigate the nature of the dominant effect, we compared methylomes of transgenic R1wtDnmt1 and R1Dnmt1Y495C mouse embryonic stem cells (mESCs) overexpressing WT and the mutant mouse proteins respectively, with the R1 (wild-type) cells.. In case of R1Dnmt1Y495C, 15 out of the 20 imprinting control regions were hypomethylated with transcript level dysregulation of multiple imprinted genes in ESCs and neurons. Software:Article Title: DNMT1 Y495C mutation interferes with maintenance methylation of imprinting control regions. Article Snippet: Hereditary Sensory and Autonomic Neuropathy Type 1E (HSAN1E) is a rare autosomal dominant neurological disorder due to missense mutations in DNA methyltransferase 1 (DNMT1).. To investigate the nature of the dominant effect, we compared methylomes of transgenic R1wtDnmt1 and R1Dnmt1Y495C mouse embryonic stem cells (mESCs) overexpressing WT and the mutant mouse proteins respectively, with the R1 (wild-type) cells.. In case of R1Dnmt1Y495C, 15 out of the 20 imprinting control regions were hypomethylated with transcript level dysregulation of multiple imprinted genes in ESCs and neurons. |