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Open AccessHighly AccessResearch article

Identification and analysis of miRNAs in human breast cancer and teratoma samples using deep sequencing

Sanne Nygaard1,2 email, Anders Jacobsen1,2 email, Morten Lindow1,2,7 email, Jens Eriksen3 email, Eva Balslev4 email, Henrik Flyger5 email, Niels Tolstrup6 email, Søren Møller6 email, Anders Krogh1 email and Thomas Litman6 email

1The Bioinformatics Centre, Department of biology, University of Copenhagen, 2200 Copenhagen N, Denmark

2The Biotech Research and Innovation Centre (BRIC), Department of biology, University of Copenhagen, 2200 Copenhagen N, Denmark

3Laboratory of Oncology, Herlev University Hospital, 2730 Herlev, Denmark

4Department of Pathology, Herlev University Hospital, 2730 Herlev, Denmark

5Department of Breast Surgery, Herlev University Hospital, 2730 Herlev, Denmark

6Exiqon A/S, Bygstubben 9, 2950 Vedbæk, Denmark

7Santaris Pharma A/S, Bøge Allé 3-5, 2970 Hørsholm, Denmark

author email corresponding author email

BMC Medical Genomics 2009, 2:35doi:10.1186/1755-8794-2-35

Published: 9 June 2009

Additional files

Additional file 1:

Figures of expression of novel miRNA loci. Expression is shown for all the putative novel miRNAs described in this paper. Each figure shows the genomic coordinates (top row), location of the approximate predicted precursor hairpin (second row: grey box = mature, white box = miRNA*), and all reads mapped to the region. Each bar represents one specific read. The bars are colour coded according to samples and expression, as labeled in each figure. Thick bars represent perfect matches, thin bars imperfect matches. Note that the approximate miRNA* (white box) is a computational construct, not the actual biological miRNA* expected from the locus. This file is best viewed on-screen.

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Additional file 2:

Figure of signed end variation of miRNAs. The 219 expressed known mature miRNAs with a minimum expression count of 3. A) The distribution of mean (signed) deviations from the most frequent mature miRNA 5' end (56 miRNAs with a 5' deviation of 0 are omitted for plotting purposes, minus denotes shorter sequences). B) The distribution of mean (signed) deviations from the most frequent mature miRNA 3' end, minus denoting shorter sequences. Ten miRNAs with a 3' deviation of 0 are omitted.

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Additional file 3:

Figures of miRNA-like expression from other ncRNA genes. Two examples of read expression patterns in predicted hairpins in non-miRNA ncRNAs. First example is within a C/D box snoRNA U3 gene (five such genes are repeated on chromosome 17). A dominant read of approximate size 22 is observed. Second example is within a 18S rRNA related pseudogene. Despite a diffuse expression pattern, there is a dominant species of read. Legend: Each figure shows the genomic coordinates (top row), location of the approximate predicted precursor hairpin (second row: grey box = mature, white box = miRNA*), and all reads mapped to the region. Each bar represents one specific read. The bars are colour coded according to samples and expression, as labeled in each figure. Thick bars represent perfect matches, thin bars imperfect matches. Note that the approximate miRNA* (white box) is a computational construct, not the actual biological miRNA* expected from the locus. This file is best viewed on-screen.

Format: PDF Size: 23KB Download file

This file can be viewed with: Adobe Acrobat Reader


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