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Sample GSM16583 Query DataSets for GSM16583
Status Public on Jun 28, 2004
Title tudor male vs tudor female-17b
Sample type RNA
 
Channel 1
Source name Adult tud[1] bw[1]sp[1] Male
Organism Drosophila melanogaster
Extracted molecule total RNA
 
Channel 2
Source name Adult tud[1] bw[1]sp[1] Female
Organism Drosophila melanogaster
Extracted molecule total RNA
 
 
Description Germlineless adult Drosophila melanogaster tud[1] bw[1]sp[1] progeny of tud[1] bw[1]sp[1] mothers were grown at 25C on GIF medium (KD Medical, Columbia, MD) for 3 to 5 days post eclosion. Whole flies were quick frozen on Dry ice and total RNA was extracted (Andrews et al, Genome Research 10:2030-2043) using Trizol reagent (GibcoBRL, Gaithersburg, MD). Probes were labeled with Cy3 (Probe 1) or Cy5 (Probe 2). To synthesize probes, mRNA was isolated by a single round of poly(A) selection using Oligotex resin (Qiagen, Valencia, CA). The purified mRNA was quantified using RiboGreen dye (Molecular Probes) in a fluorescent assay. RiboGreen dye was diluted 1:200 (v/v final) and mixed with known RNA concentrations (determined by absorbance at 260 nm) ranging from 1 to 5000 ng/ml. A Millennium RNA size ladder (Ambion, Austin, TX) was used to generate standard curves and unknown samples were diluted as necessary. Fluorescence was measured in 96-well plates with a FLUOstar fluorometer (BMG Lab Technologies, Germany) fitted with 485 nm (excitation) and 520 nm (emission) filters. Between 25 and 100 ng mRNA were separated on an Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA), to examine the mRNA size distribution. 200 ng of purified mRNA were converted to either a Cy3- or Cy5-labeled cDNA probe using a custom labeling kit (Incyte Genomics). Each reaction contained 50 mM Tris–HCl pH 8.3, 75 mM KCl, 15 mM MgCl2, 4 mM DTT, 2 mM dNTPs (0.5 mM each), 2 µg Cy3 or Cy5 random 9mer (Trilink, San Diego, CA), 20 U RNase inhibitor (Ambion), 200 U MMLV RNase H-free reverse transcriptase (Promega, Madison, WI) and mRNA. Correspondingly labeled Cy3 and Cy5 cDNA products were combined and purified on a size exclusion column, concentrated by ethanol precipitation and resuspended in hybridization buffer. Probes were added between two subarray slides and developed as described (Yue et al.2001, NAR. 29:e41). Microarrays were scanned on a GenePix 4000A scanner (Axon Instruments, Foster City, CA) at 535 nm. Signal intensities were initially stored and analyzed using GEMTools software (Incyte Genomics, Palo Alto CA). Background corrections were done by calculating the average Cy3/Cy5 signal to produce a balanced coefficient (Yue et al., 2001) Further corrections for non-uniform conditions during array printing and/or hybridization were performed using Qualifier software (Novation Bioscience, Palo Alto CA).
 
Submission date Feb 06, 2004
Last update date Apr 25, 2012
Contact name Brian Oliver
E-mail(s) briano@nih.gov
Phone 301-204-9463
Organization name NIDDK, NIH
Department LBG
Lab Developmental Genomics
Street address 50 South Drive
City Bethesda
State/province MD
ZIP/Postal code 20892
Country USA
 
Platform ID GPL20
Series (1)
GSE442 Sex-biased gene expression

Data table header descriptions
ID_REF
LnCy3DA2 Natural log transformed intensity signal from Cy3 channel. Values are corrected using Qualifier software by taking a moving average across the entire signal range
LnCy5DA2 Natural log transformed intensity signal from Cy5 channel. Values are corrected using Qualifier software by taking a moving average across the entire signal range
VALUE Natural log transformed ratio of corrected Cy3/Cy5 signal calculated by taking the corrected LnCy3DA2 signal value and subtracting the LnCy5DA2 signal value for each array element
DiffExpr Ratio of uncorrected Probe 1/Probe 2 signal intensity
BalancedDiffExpr Ratio of uncorrected Probe 1/balanced Probe 2 signal intensity
Probe 1 Signal Raw signal intensity data from Cy3 (Probe 1) channel
Probe 1S/B Probe 1 signal minus background/background
Probe 1 Area% Percentage of area read from element spot
Probe 2 BalancedSignal Raw signal intensity data from Cy5 channel balanced against Probe 1 signal. Intensity is adjusted by a balancing coefficient that takes the average Cy3 signal on an array/the average Cy5 signal on the array
Probe 2 Signal Raw signal intensity data from Cy5 (Probe 2) channel
Probe 2 S/B Probe 2 signal-background/background
Probe 2 Area% Percentage of area read from element spot

Data table
ID_REF LnCy3DA2 LnCy5DA2 VALUE DiffExpr BalancedDiffExpr Probe 1 Signal Probe 1S/B Probe 1 Area% Probe 2 BalancedSignal Probe 2 Signal Probe 2 S/B Probe 2 Area%
1 2.84 2.99 -0.14 -1.1 -1.3 18427 122.2 72 23739 20824 161.2 72
2 1.85 1.07 0.77 2.2 1.9 6899 47.6 75 3575 3136 25.3 75
3 1.47 0.77 0.7 2 1.8 4793 33.2 81 2696 2365 18.9 81
4 2.76 2.1 0.66 1.9 1.7 17382 117.7 74 10477 9190 71.2 74
5 2.72 2.8 -0.07 -1 -1.2 17359 118.3 71 20640 18105 140.3 71
6 2.25 2.57 -0.32 -1.3 -1.5 11187 77.1 75 16413 14397 111.7 75
7 2.17 2.18 -0.005129674 1 -1.1 10262 71.8 74 11430 10026 80.6 74
8 1.49 1.55 -0.06 -1 -1.2 5207 37.9 76 6226 5461 45.8 76
9 0.67 0.59 0.07 1.2 1 2409 18.5 65 2350 2061 18.2 65
10 -0.95 -0.71 -0.23 -1.2 -1.4 357 3.5 94 490 430 4.5 94
11 -1.06 -1.07 0.002548423 1 -1.1 321 4.1 100 351 308 4.5 100
12 -1.16 -1.05 -0.11 -1 -1.2 301 3.8 100 356 312 4.4 100
13 -1.23 -1.33 0.09 1.1 1 279 3.5 100 279 245 3.6 100
14 -0.37 -0.27 -0.1 -1.1 -1.3 653 6.7 82 826 725 8.6 82
15 -0.22 -0.2 -0.01 -1 -1.1 782 8 81 893 783 9.5 81
16 0.31 0.28 0.02 -1 -1.1 1320 12.8 88 1510 1325 14.9 88
17 143 2.3 100 133 117 2.2 100
18 108 1.9 95 97 85 1.9 95
19 -0.27 -0.48 0.21 1.3 1.1 793 7.9 82 700 614 7.1 82
20 -1.53 -1.37 -0.16 -1.1 -1.2 230 3.1 100 287 252 3.7 100

Total number of rows: 31464

Table truncated, full table size 1572 Kbytes.




Supplementary data files not provided

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