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Platform GPL1783 Query DataSets for GPL1783
Status Public on Jan 07, 2005
Title DmelWhiteLab2003Jul30_r40
Technology type spotted DNA/cDNA
Distribution non-commercial
Organism Drosophila melanogaster
 
Description PCR fragment spotted array with 95% of the genes in D. melanogaster BDGP release 4.0 Array has 8 rows of 4 blocks each, numbered 1-32 starting in the upper left and ending in the lower right. 16 pins used to print. Each KP is only spotted once.
KP# annotation file files used: isPcr: http://www.soe.ucsc.edu/~kent/src/ options -out=bed -maxSize=1500 accessed: 22 Dec 04
D. mel. euchromatin release 4: ftp://ftp.fruitfly.org/pub/download/compressed/na_euchromatin_genomic_dmel_RELEASE4.FASTA.gz accessed: 22 Dec 04
D. mel. .gff annotation files by chromosome: ftp://flybase.net/genomes/Drosophila_melanogaster/current/gff/dmel-[CHR]-r4.0.gff.gz accessed 22 Dec 04
D. mel. .fasta transcript and gene files: ftp://flybase.net/genomes/Drosophila_melanogaster/current/fasta/dmel-all-[transcript/gene]-r4.0.fasta.gz accessed 22 Dec 04
Heterochromatin from release hetr32b: ftp://flybase.net/genomes/Drosophila_melanogaster/current_hetchr/ accessed 28 Dec 04
Used dmel-all-chromosome.hetr32b.fasta and similar files as above
r4.0 euchromatin extends into heterochromatin. However, genes.gff files don't seem to yet. So some KPs may have multiple chromosomes listed e.g. 2h,2R but are still good.
Gene calls are based first on transcripts (isPcr.transcript file). So if a probe hits an intron in gene A on the + strand and transcript in gene B on the - strand, it will call it for gene B
If it hits no transcripts but it hits a gene, it calls it for that gene (this is slightly inconsistent in how complete we regard the annotation)
In PCR_results field, I don't have the data for the KPST genes so I filled these in with 1MB (1 maybe) except for KPST3 (dpp) which apparently did not work. Note that KPST8 is GFP.
Note also that for some genes the PCR_results says 2 or more bands, but it is flagged good. For these, there were 2 or more hits in the same transcript in the genome, so we'd expect multiple bands.
Fields should be self-explanatory except SPOT_GROUP. These are KPs which hit the same transcript with one catch: singletons are left alone.
If KP1, KP2, KP3, KP4, and KP5 are probes and T1-5 are transcripts of a gene ('{' means contained in) and KP1{T1,T5 KP2{T2, KP3{T2,T3 , KP4{T3,T4, KP5{T2 then:
The spot groups will be [KP1], [KP2,KP5], [KP3,KP4]
Keywords = spotted, PCR product, Drosophila melanogaster
 
Submission date Jan 04, 2005
Last update date May 26, 2005
Contact name Scott A Rifkin
Phone 617-496-5540
URL http://kim.bio.upenn.edu/~scott/
Organization name Harvard University
Department OEB
Lab Hartl Lab
Street address 16 Divinity Ave
City Cambridge
State/province MA
ZIP/Postal code 02138
Country USA
 
Samples (12) GSM50438, GSM50439, GSM50446, GSM50448, GSM50454, GSM50455 
Series (1)
GSE2642 Evolution of gene expression in the Drosophila melanogaster subgroup update and extension

Data table header descriptions
ID
FBgn Flybase gene name
LAB_ID KP: internal lab identifier, specific to individual primer groups. Use this for communicating with the White lab.
BLOCK block on the array (see platform description)
ROW row in the block (max = 25)
COLUMN column in the block (max = 25)
TYPE type of spot (blank, coding sequence, tiling, etc.)
FLAG bad spot either because PCR didn't work or hit (computationally) multiple spots or gene was problematic
SPOT_GROUP other spots which probe the same or overlapping transcripts
CG Computed gene number (see http://flybase.bio.indiana.edu/docs/nomenclature/lk/nomenclature.html
TRANSCRIPTS transcripts which the spot measures
CHROMOSOME chromosome of the gene
STRAND plus strand or minus strand
FORWARD_PRIMER forward primer for the PCR product
REVERSE_PRIMER reverse primer for the PCR product
96WELL_PLATE Location in the 96 well primer plates
384WELL_PLATE Location in the 384 well plates used for printing
LOCATION_IN_CHROMOSOME location of probe in the chromosome
LOCATION_IN_CG location of probe in the gene
LOCATION_IN_TRANSCRIPT location of probe in the transcript
CLONE_ID
ORF
SPOT_ID

Data table
ID FBgn LAB_ID BLOCK ROW COLUMN TYPE FLAG SPOT_GROUP CG TRANSCRIPTS CHROMOSOME STRAND FORWARD_PRIMER REVERSE_PRIMER 96WELL_PLATE 384WELL_PLATE LOCATION_IN_CHROMOSOME LOCATION_IN_CG LOCATION_IN_TRANSCRIPT CLONE_ID ORF SPOT_ID
0 BLANK BLANK 1 1 1 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
1 BLANK BLANK 1 1 2 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
2 BLANK BLANK 1 1 3 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
3 BLANK BLANK 1 1 4 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
4 BLANK BLANK 1 1 5 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
5 BLANK BLANK 1 1 6 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
6 BLANK BLANK 1 1 7 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
7 BLANK BLANK 1 1 8 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
8 BLANK BLANK 1 1 9 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
9 BLANK BLANK 1 1 10 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
10 BLANK BLANK 1 1 11 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
11 BLANK BLANK 1 1 12 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
12 BLANK BLANK 1 1 13 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
13 BLANK BLANK 1 1 14 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
14 BLANK BLANK 1 1 15 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
15 BLANK BLANK 1 1 16 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
16 BLANK BLANK 1 1 17 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
17 BLANK BLANK 1 1 18 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
18 BLANK BLANK 1 1 19 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK
19 BLANK BLANK 1 1 20 blank flagged NA NA NA NA NA NA NA NA NA NA NA NA BLANK

Total number of rows: 20000

Table truncated, full table size 3964 Kbytes.






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