Table of Contents

guest
2024-04-18
Welcome to the LINCS PCCSE!
LINCS PCCSE Overview
   SAB Materials
LINCS PCCSE Data Processing and Levels
Internal standards used in P100
Internal standards used in GCP
GCT Download
LINCS PCCSE Data Quick Access Table
Create Custom GCT

Welcome to the LINCS PCCSE!


WELCOME TO THE LINCS PCCSE PANORAMA REPOSITORY

This is the LINCS Proteomic Characterization Center for Signaling and Epigenetics (PCCSE) Panorama Repository for the reduced representation phosphoproteomics assay ("P100") and global chromatin profiling assay ("GCP") primary mass chromatogram data. Our center makes systematic perturbations (drug treatments, gene disruption/editing, and directed differentiation) in a variety of biological models including cancer and neurodevelopment. We read out molecular changes in the cells in the spaces of phosphosignaling (P100) and histone modification (GCP). In collaboration with the LINCS Center for Transcriptomics, we also read out changes in transcription using their L1000 assay. Look here for more information about our center or download our poster here.

PCCSE EXPERIMENTAL PARADIGMS ANNOUNCING THE PCCSE PROTEOMICS CONNECTIVITY HUB
PCCSE Data Generation Paradigms CLUE Proteomics Hub

Go beyond the heatmaps!  Explore connections and relationships among our perturbations in the Proteomics Connectivity Hub, a collaboration with the Connectivity Map Project.  Free account creation required.

NEW! ASMS 2017 Poster from our group!




LINCS PCCSE Overview





SAB Materials


Scientific Advisory Board Meetings + Slide Decks

August 2016 SAB Meeting

October 2016 SAB Meeting

December 2016 SAB Meeting (agenda for 12/9/2016)

 

LINCS PCCSE Background Materials

PCCSE Guide

 

LINCS PCCSE Publications

Creech et al., Global Chromatin Profiling

Abelin et al., Reduced-representation Phosphoproteomics

 

LINCS PCCSE Presentations (Talks & Posters)

LINCS PCCSE Center Update - Jaffe et al.- LINCS Annual Meeting - NIH - September 2016 (slide deck)

Proteomic Connectivity - Litichevskiy et al.- LINCS Annual Meeting - NIH - September 2016 (poster)

Proteomic Profiling in Neuronal Systems - Young et al.- LINCS Annual Meeting - NIH - September 2016 (poster)

Proteomic Profiling in Cardiovascular Systems - Gopal et al., LINCS Annual Meeting - NIH - September 2016 (poster)

Unlocking Next-generation DIA MS Data for LINCS - Egertson et al., LINCS Annual Meeting - NIH - September 2016 (poster)

 




LINCS PCCSE Data Processing and Levels


LINCS PCCSE Data Processing and Levels

LINCS espouses the concept of making different data levels available for public use.  Different data levels correspond different steps along our processing workflow.  The LINCS PCCSE levels are defined as follows:

Level 0 - Raw Mass Spectrometry Data (LCMS) - will be available through a chorusproject.org repository in the future

Level 1 - Probe Reads (SKY) - Curated Skyline documents; available on this website, including metadata

Level 2 - Raw Numerical Data (RPT) - Matrix data of extracted signal ratios of endogenous probes vs. internal standards (log2 transformed); available on this website, including metadata

Level 3 - Normalized and QC'ed Numerical Data (QCNORM) - Matrix data derived from Level 2 after automated processing and normalization

Level 4 - Differential Quantification (DIFF) - Matrix data of Level 3 with plate-wide median ratio of each analyte subtracted from each sample; available on this website, including metadata 

These data levels are mapped onto our processing pipeline as depicted below:

TIP: To browse and access our data sets, hover over the "LINCS" folder in the upper left corner:








Internal standards used in P100


96 modified peptide sequences of internal standards used in P100 assay:

 

ALGS[+80]PTKQLLPC[+57]EMAC[+57]NEK
VSMPDVELNLKS[+80]PK
LGPGRPLPTFPTSEC[+57]TS[+80]DVEPDTR
LPLVPES[+80]PRR
S[+80]FAGNLNTYKR
S[+122]DKPDMAEIEKFDK
S[+122]DKPDM[+16]AEIEKFDK
QDDS[+80]PPRPIIGPALPPGFIK
VYT[+80]HEVVTLWYR
KPNIFYSGPAS[+80]PARPR
AFGSGIDIKPGT[+80]PPIAGR
LAAPSVSHVS[+80]PR
QGSGRES[+80]PSLASR
IHVSRS[+80]PTRPR
TNPPTQKPPS[+80]PPMSGR
S[+80]PPAPGLQPMR
S[+80]PPAPGLQPM[+16]R
RPHS[+80]PEKAFSSNPVVR
SEVQQPVHPKPLS[+80]PDSR
NEEPVRS[+80]PERR
LFIIRGS[+80]PQQIDHAK
DRS[+80]SPPPGYIPDELHQVAR
LGMLS[+80]PEGTC[+57]K
LGM[+16]LS[+80]PEGTC[+57]K
RNS[+80]SEASSGDFLDLK
AAPEAS[+80]SPPASPLQHLLPGK
TPKDS[+80]PGIPPSANAHQLFR
RLS[+80]ESQLSFRR
SMS[+80]VDLSHIPLKDPLLFK
S[+80]PTGPSNSFLANMGGTVAHK
S[+80]LTNSHLEKK
SPDKPGGS[+80]PSASRR
IGPLGLS[+80]PK
A[+42]TTATMATSGS[+80]AR
A[+42]TTATM[+16]ATSGS[+80]AR
SSDQPLTVPVS[+80]PK
VLS[+80]PTAAKPSPFEGK
ETPHS[+80]PGVEDAPIAK
FYETKEESYS[+80]PSKDR
HLPS[+80]PPTLDSIITEYLR
RLS[+80]QSDEDVIR
ATS[+80]PVKSTTSITDAK
LENS[+80]PLGEALR
ISNLS[+80]PEEEQGLWK
RLIS[+80]PYKK
TLGRRDS[+80]SDDWEIPDGQITVGQR
IYQY[+80]IQSR
ANS[+80]PEKPPEAGAAHKPR
RLS[+80]LPGLLSQVSPR
IHS[+80]PIIR
DLVQPDKPAS[+80]PK
TFS[+80]LTEVR
S[+80]IQDLTVTGTEPGQVSSR
LHS[+80]APNLSDLHVVRPK
S[+122]DNGELEDKPPAPPVR
HAS[+80]PILPITEFSDIPR
LIPGPLS[+80]PVAR
LEVTEIVKPS[+80]PK
ST[+80]FHAGQLR
SNS[+80]LPHSAVSNAGSK
SPALKS[+80]PLQSVVVR
TPS[+80]IQPSLLPHAAPFAK
SQS[+80]PHYFR
HRPS[+80]PPATPPPK
S[+80]IPLSIK
VGS[+80]LDNVGHLPAGGAVK
SPS[+80]PAHLPDDPKVAEK
ANAS[+80]PQKPLDLK
VLS[+80]PLIIK
LLEDS[+80]EESSEETVSR
TQLWASEPGT[+80]PPLPTSLPSQNPILK
NDS[+80]WGSFDLR
KAYS[+80]FC[+57]GTVEYMAPEVVNR
KAYS[+80]FC[+57]GTVEYM[+16]APEVVNR
SLVGS[+80]WLK
SDS[+80]PENKYSDSTGHSK
SFS[+80]ADNFIGIQR
ANS[+80]FVGTAQYVSPELLTEK
RRLS[+80]SLR
QIT[+80]MEELVR
QIT[+80]M[+16]EELVR
YGS[+80]PPQRDPNWNGER
SFS[+80]SQRPVDR
SST[+80]PLPTISSSAENTR
AGS[+80]PDVLR
S[+80]LTAHSLLPLAEK
TEFLDLDNSPLSPPS[+80]PR
VDDDS[+80]LGEFPVTNSR
YLLGDAPVS[+80]PSSQK
ALPQT[+80]PRPR
TAPTLS[+80]PEHWK
LAS[+80]PELER
LQS[+80]EPESIR
LQTPNT[+80]FPKR
SLS[+80]LGDKEISR
S[+80]IEVENDFLPVEK

 




Internal standards used in GCP


79 modified peptide sequences of internal standards used in GCP assay:

 

T[+56]K[+56]QTAR
T[+56]K[+70]QTAR
T[+56]K[+28]QTAR
T[+56]K[+42]QTAR
T[+56]K[+42]QTAR
K[+112.1]STGGK[+56]APR
K[+126.1]STGGK[+56]APR
K[+84.1]STGGK[+56]APR
K[+98.1]STGGK[+56]APR
K[+98]STGGK[+56]APR
K[+112.1]STGGK[+42]APR
K[+126.1]STGGK[+42]APR
K[+84.1]STGGK[+42]APR
K[+98.1]STGGK[+42]APR
K[+98]STGGK[+42]APR
K[+112.1]S[+80]TGGK[+56]APR
K[+126.1]S[+80]TGGK[+56]APR
K[+84.1]S[+80]TGGK[+56]APR
K[+98.1]S[+80]TGGK[+56]APR
K[+98]S[+80]TGGK[+56]APR
K[+112.1]S[+80]TGGK[+42]APR
K[+126.1]S[+80]TGGK[+42]APR
K[+84.1]S[+80]TGGK[+42]APR
K[+98.1]S[+80]TGGK[+42]APR
K[+98]S[+80]TGGK[+42]APR
K[+112.1]QLATK[+56]AAR
K[+98]QLATK[+56]AAR
K[+112.1]QLATK[+42]AAR
K[+98]QLATK[+42]AAR
K[+226.1]QLATK[+56]AAR
K[+112.1]QLATK[+170.1]AAR
K[+112.1]SAPATGGVK[+56]K[+56]PHR
K[+112.1]SAPATGGVK[+70]K[+56]PHR
K[+112.1]SAPATGGVK[+28]K[+56]PHR
K[+112.1]SAPATGGVK[+42]K[+56]PHR
K[+126.1]SAPATGGVK[+56]K[+56]PHR
K[+126.1]SAPATGGVK[+70]K[+56]PHR
K[+126.1]SAPATGGVK[+28]K[+56]PHR
K[+126.1]SAPATGGVK[+42]K[+56]PHR
K[+84.1]SAPATGGVK[+56]K[+56]PHR
K[+84.1]SAPATGGVK[+70]K[+56]PHR
K[+84.1]SAPATGGVK[+28]K[+56]PHR
K[+84.1]SAPATGGVK[+42]K[+56]PHR
K[+98.1]SAPATGGVK[+56]K[+56]PHR
K[+98.1]SAPATGGVK[+70]K[+56]PHR
K[+98.1]SAPATGGVK[+28]K[+56]PHR
K[+98.1]SAPATGGVK[+42]K[+56]PHR
K[+98]SAPATGGVK[+56]K[+56]PHR
K[+98]SAPATGGVK[+70]K[+56]PHR
K[+98]SAPATGGVK[+28]K[+56]PHR
K[+98]SAPATGGVK[+42]K[+56]PHR
K[+112.1]SAPSTGGVK[+56]K[+56]PHR
Y[+56]RPGTVALR
Y[+56]QK[+56]STELLIR
Y[+56]QK[+70]STELLIR
Y[+56]QK[+28]STELLIR
Y[+56]QK[+42]STELLIR
E[+56]IAQDFK[+56]TDLR
E[+56]IAQDFK[+70]TDLR
E[+56]IAQDFK[+28]TDLR
G[+56]K[+56]GGK[+56]GLGK[+56]GGAK[+56]R
G[+56]K[+42]GGK[+56]GLGK[+56]GGAK[+56]R
G[+56]K[+56]GGK[+56]GLGK[+42]GGAK[+56]R
G[+56]K[+56]GGK[+56]GLGK[+56]GGAK[+42]R
G[+56]K[+56]GGK[+56]GLGK[+56]GGAK[+70]R
G[+56]K[+42]GGK[+42]GLGK[+56]GGAK[+56]R
G[+56]K[+42]GGK[+56]GLGK[+56]GGAK[+42]R
G[+56]K[+56]GGK[+42]GLGK[+42]GGAK[+56]R
G[+56]K[+56]GGK[+56]GLGK[+42]GGAK[+42]R
G[+56]K[+56]GGK[+42]GLGK[+42]GGAK[+42]R
G[+56]K[+42]GGK[+42]GLGK[+42]GGAK[+56]R
G[+56]K[+42]GGK[+42]GLGK[+56]GGAK[+42]R
G[+56]K[+42]GGK[+42]GLGK[+42]GGAK[+42]R
D[+56]AVTYTEHAK[+56]R
K[+112.1]VLR
K[+126.1]VLR
K[+84.1]VLR
K[+98.1]VLR
A[+56]GLQFPVGR

 




GCT Download


FileDownload



LINCS PCCSE Data Quick Access Table


Quick Links (Levels 1,2,4 data):

ALL P100 DATA  ALL GCP DATA 

 

Quick Level 4 Data Visualization (& Download):

Note: this is probably what you want!  For rapid access to visualizations of data, use the table below. Clicking on any link will lead to a visualization of data that we have collected. Each cell is a plate ID number followed by links to the data where available. Links beginning with "P" point to P100 data, while links beginning with "G" point to GCP data. The numbers after the leading character describe length of compound treatment before samples were harvested. All P100 data is acquired in DIA unless otherwise marked.

  MCF7 PC3 A549 A375 YAPC NPC Astrocytes
Epigenetically-active drugs 15 P3/G24 18 P3/G24 19 P3/G24 17 P3/G24 30 P3/G24 16 P3/G24 64 P3/G24
Neurodevelopmental drugs 23 P3/G24 24 P3/G24 25 P3/G24 22 P3/G24 31 P3/G24 20 P3/G24 65 P3/G24
Kinase/Pathway Inhibitors 29 P3/P6/P24/G24 34 P3/G24 33 P3/G24 28 P3/G24 32 P3/G24 27 P3/G24 66 P3/G24
Cardiotoxic drugs 60 P3/G24 61 P3/G24 58 P3/G24 59 P3/G24 62 P3/G24 63 P3/G24 67 P3/G24

Click here for more information on LINCS PCCSE Data Levels.

CUSTOM SUBSETTING OF

LEVEL 4 P100 DATA

CUSTOM SUBSETTING OF

LEVEL 4 GCP DATA




Create Custom GCT


Select replicate annotations
Include files in subfolders