Schema for TSRchitect RAMPAGE Embryos TSS - TSRchitect RAMPAGE Embryos Transcription Start Sites
  Database: dm6    Primary Table: tss_RAMPAGE_Dmel23_E23h Data last updated: 2021-04-19
Big Bed File: /gbdb/dm6/bbi/RAMPAGE_dedup/tsrchitect/Dmel23_E23h_tsrchitect.bb
Item Count: 3,289
Format description: RAMPAGE Peaks Identified by TSRchitect
fieldexampledescription
chromchr2LReference sequence chromosome or scaffold
chromStart16251772Start position in chromosome
chromEnd16251776End position in chromosome
nametsr_peaked_447Name of RAMPAGE peak
score730Score from 0-1000
strand-+ or -
nTSSs2Count of TSSs
nTAGs110Count of tags
tsrPeak0.73Maximum tag count fraction for all TSS positions in the TSR
tsrWdth4Width of TSR
tsrTrq0.68TSR torque; measure of TSR balance
tsrSI1.15Shape index (SI) value of TSR
tsrMSI0.15Modified shape index (MSI) value of TSR

Sample Rows
 
chromchromStartchromEndnamescorestrandnTSSsnTAGstsrPeaktsrWdthtsrTrqtsrSItsrMSI
chr2L1625177216251776tsr_peaked_447730-21100.7340.681.150.15
chr2L1626169216261693tsr_peaked_4481000-1501.0010.002.001.00
chr2L1628772716287728tsr_peaked_4491000-1251.0010.002.001.00
chr2L1630291416302915tsr_peaked_4501000-1381.0010.002.001.00
chr2L1630737116307372tsr_peaked_2011000+1261.0010.002.001.00
chr2L1631069116310711tsr_peaked_451700-21080.7020-3.871.120.12
chr2L1632561316325614tsr_peaked_4521000-1371.0010.002.001.00
chr2L1635260016352601tsr_peaked_4531000-1771.0010.002.001.00
chr2L1635262016352621tsr_peaked_4541000-1821.0010.002.001.00
chr2L1644733716447338tsr_peaked_2021000+1401.0010.002.001.00

TSRchitect RAMPAGE Embryos TSS (tss_RAMPAGE_embryos) Track Description
 

Description

This track shows the locations of putative Transcription Start Sites (TSS) in the D. melanogaster genome based on the analysis of RAMPAGE data from different embryonic stages in one-hour intervals.

The embryos RAMPAGE datasets were retrieved from the Gene Expression Omnibus database at NCBI under the accession numbers GSE36212 and GSE89299. The RAMPAGE reads were mapped against the D. melanogaster (dm6) assembly using STAR. The putative promoter regions were identified by TSRchitect.

References

Dobin A, Davis CA, Schlesinger F, Drenkow J, Zaleski C, Jha S, Batut P, Chaisson M, Gingeras TR. STAR: ultrafast universal RNA-seq aligner. Bioinformatics. 2013 Jan 1;29(1):15-21.

Batut P, Dobin A, Plessy C, Carninci P, Gingeras TR. High-fidelity promoter profiling reveals widespread alternative promoter usage and transposon-driven developmental gene expression. Genome Res. 2013 Jan;23(1):169-80.