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Detecting differentially methylated mRNA from MeRIP-Seq with likelihood ratio test
2014 IEEE Global Conference on Signal and Information Processing (GlobalSIP), 2014The study of mRNA methylation is an emerging research field greatly fueled by recent advancement in high throughput sequencing technology. We propose here a binomial likelihood ratio test ("bltest") aiming at detecting differentially methylated mRNA with MeRIP-Seq data, "bltest" models the read counts of each RNA methylation site in IP and input ...
Lin Zhang +6 more
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Modeling of replicates variances for detecting RNA methylation site in MERIP-SEQ data
2015 IEEE China Summit and International Conference on Signal and Information Processing (ChinaSIP), 2015The recent advent of the state-of-art high throughput sequencing technology, known as Methylated RNA immunoprecipitation (IP) sequencing (MeRIP-Seq), provided the biologists the first global view of epigenetic modifications on the transcriptome at a high resolution.
Xiaodong Cui +3 more
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These are the codes for MeRIP-seq/scRNA-seq analysis used in the paper titled "METTL3-Driven RNA Modifications: A Key Mechanism and Potential Therapeutic Target in Pancreatic Acinar Cell Carcinoma in Mice". The relevant GEO accession numbers are as follows: GSE305529, GSE305530.
Tatekawa, Shotaro +4 more
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Tatekawa, Shotaro +4 more
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MeRIP-Seq for Identifying Stress-Responsive Transcriptome-Wide m6A Profiles in Plants
Recent advancements in detection and mapping methods have enabled researchers to uncover the biological importance of RNA chemical modifications, which play a vital role in post-transcriptional gene regulation. Although numerous types of RNA modifications have been identified in higher eukaryotes, only a few have been extensively studied for their ...Ganesan, Govindan, Ramanjulu, Sunkar
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International Journal of Biological Macromolecules
Chinese hamster ovary (CHO) cells remain the primary host system for recombinant therapeutic protein production. Enhancing transgene expression efficiency while maintaining stable production persists as a key challenge in CHO cell engineering. While N6-methyladenosine (m6A) modification - the most abundant RNA methylation - regulates RNA stability and ...
Wen, Wang +10 more
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Chinese hamster ovary (CHO) cells remain the primary host system for recombinant therapeutic protein production. Enhancing transgene expression efficiency while maintaining stable production persists as a key challenge in CHO cell engineering. While N6-methyladenosine (m6A) modification - the most abundant RNA methylation - regulates RNA stability and ...
Wen, Wang +10 more
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Comparative Biochemistry and Physiology Part D: Genomics and Proteomics
As a widely epigenetic modification, m6A (N6-methyladenosine, m6A) can regulate the degradation, translation, and other biological functions of circRNAs through dynamic reversible processes. It plays an important role in regulating the life activities of biological organisms, particularly in cell differentiation, apoptosis, embryonic development ...
Ru, Zhang +9 more
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As a widely epigenetic modification, m6A (N6-methyladenosine, m6A) can regulate the degradation, translation, and other biological functions of circRNAs through dynamic reversible processes. It plays an important role in regulating the life activities of biological organisms, particularly in cell differentiation, apoptosis, embryonic development ...
Ru, Zhang +9 more
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Theoretical and Natural Science
Abstract. N6-methyladenosine (m6A), recognized as the most prevalent post-transcriptional modification in organisms, has been substantiated to exert a significant influence on the genetic mechanisms underlying breast cancer. To delve deeper into the disparities in expression, modification, and interactions between mRNA and m6A in breast cancer (BC), we
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Abstract. N6-methyladenosine (m6A), recognized as the most prevalent post-transcriptional modification in organisms, has been substantiated to exert a significant influence on the genetic mechanisms underlying breast cancer. To delve deeper into the disparities in expression, modification, and interactions between mRNA and m6A in breast cancer (BC), we
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