miRNA and other small RNAs
1
0
Entering edit mode
Wu, Huiyun ▴ 70
@wu-huiyun-5271
Last seen 9.7 years ago
Dear users, I have a question about miRNA differential profiling between two groups. Someone suggested a further filtering of other small RNAs such as mRNA degradation, etc with lengths similar to miRNA after BAM file (which pre-filtering out longer or shorter ones) read-in. I was wondering what consequences would be if I do NOT conduct this process. In this situation, a miRNA count table contains those contaminated non-coding small RNAs and those small RNAs are brought into DE analysis. My intuitive understanding is that it should be fine as long as the miRNA IDs (say, Entrez IDs)are not shared by other small RNAs during alignment or annotation. thanks in advance. sincerely, William Wu [[alternative HTML version deleted]]
miRNA Alignment Annotation PROcess miRNA Alignment Annotation PROcess • 991 views
ADD COMMENT
0
Entering edit mode
@alessandroguffantigenomniacom-4436
Last seen 9.7 years ago
Hi - does not sound as a BioC question but I will be happy to answer: miRNA filtering is important because many processed tRNAs, snoRNAs, piRNAs etc are highly similar to known miRNAs. Hence their presence will screw up your counts Kind regards Alessandro ----------------------------------------------------- Alessandro Guffanti - Bioinformatics, Genomnia srl Via Nerviano, 31 - 20020 Lainate, Milano, Italy Ph: +39-0293305.702 Fax: +39-0293305.777 http://www.genomnia.com "If you can dream it, you can do it" (Walt Disney) -----Original Message----- From: "Wu, Huiyun" <william.wu@vanderbilt.edu> To: "bioconductor@r-project.org" <bioconductor@r-project.org> Date: Wed, 16 May 2012 15:52:00 -0500 Subject: [BioC] miRNA and other small RNAs Dear users, I have a question about miRNA differential profiling between two groups. Someone suggested a further filtering of other small RNAs such as mRNA degradation, etc with lengths similar to miRNA after BAM file (which pre-filtering out longer or shorter ones) read-in. I was wondering what consequences would be if I do NOT conduct this process. In this situation, a miRNA count table contains those contaminated non-coding small RNAs and those small RNAs are brought into DE analysis. My intuitive understanding is that it should be fine as long as the miRNA IDs (say, Entrez IDs)are not shared by other small RNAs during alignment or annotation. thanks in advance. sincerely, William Wu [[alternative HTML version deleted]] _______________________________________________ Bioconductor mailing list Bioconductor@r-project.org https://stat.ethz.ch/mailman/listinfo/bioconductor [https://stat.ethz.ch/mailman/listinfo/bioconductor] Search the archives: http://news.gmane.org/gmane.science.biology.informatics.conductor [http://news.gmane.org/gmane.science.biology.informatics.conductor] ----------------------------------------------------------- Il Contenuto del presente messaggio potrebbe contenere informazioni confidenziali a favore dei soli destinatari del messaggio stesso. Qualora riceviate per errore questo messaggio siete pregati di cancellarlo dalla memoria del computer e di contattare i numeri sopra indicati. Ogni utilizzo o ritrasmissione dei contenuti del messaggio da parte di soggetti diversi dai destinatari รจ da considerarsi vietato ed abusivo. The information transmitted is intended only for the per...{{dropped:10}}

Login before adding your answer.

Traffic: 419 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6