Summary of Study ST002095

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001328. The data can be accessed directly via it's Project DOI: 10.21228/M82978 This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST002095
Study TitleAddressing batch effects in large-scale metabolomics with augmented experimental design and meta-analysis (Part 1)
Study SummaryNon-polar and polar sequential extracts were collected on three groups of C. elegans: natural isolates, central metabolism mutants, and UDP-glucuronosyltrasnferase mutants. Untargeted LC-MS (HILIC/RP - positive and negative mode) and NMR (CDCl3/H2O) studies were conducted using a Vanquish UHPLC coupled to an Orbitrap Elite MS and NEO 800 MHz Bruker NMR spectrometer, respectively. An augmented design, rank transformation of the raw data, strict feature filtering and QA/QC followed by a meta-analysis was performed on all datasets to demonstrate the benefits of this analysis approach and identify stable, significant features to prioritize for downstream compound identification efforts.
Institute
University of Georgia - Complex Carbohydrate Research Center
LaboratoryEdison Lab
Last NameGarcia
First NameBrianna
Address315 Riverbend Road, Athens, GA, 30602, USA
Emailbrianna.garcia@uga.edu
Phone7065424401
Submit Date2022-02-22
Num Groups3
Total Subjects116
Study CommentsThree study groups of C. elegans strains were used: central metabolism mutants (CMM), UDP-glucuronosyltransferase (UGT) mutants, and natural isolates.
Raw Data AvailableYes
Raw Data File Type(s)fid
Analysis Type DetailNMR
Release Date2022-04-04
Release Version1
Brianna Garcia Brianna Garcia
https://dx.doi.org/10.21228/M82978
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001328
Project DOI:doi: 10.21228/M82978
Project Title:Addressing batch effects in large-scale metabolomics with augmented experimental design and meta-analysis
Project Summary:Untargeted LC-MS study conducted using RP and HILIC chromatography on three groups of C. elegans: natural isolates, central metabolism mutants, and UDP-glucuronosyltransferase mutants. An augmented study design, rank transformation of the raw data, strict QA/QC followed by a meta-analysis was used for data analysis.
Institute:University of Georgia - Complex Carbohydrate Research Center
Laboratory:Edison Lab
Last Name:Garcia
First Name:Brianna
Address:315 Riverbend Road, Athens, GA 30602
Email:brianna.garcia@uga.edu
Phone:7065424401
Funding Source:U2CES030167
Contributors:Amanda O. Shaver, Goncalo J. Gouveia, Alison M. Morse, Zihao Liu, Carter K. Asef, Ricardo M. Borges, Franklin E. Leach III, Erik C. Andersen, I. Jonathan Amster, Facundo M. Fernández, Arthur S. Edison, and Lauren M. McIntyre

Subject:

Subject ID:SU002179
Subject Type:Invertebrate
Subject Species:Caenorhabditis elegans
Taxonomy ID:6239

Factors:

Subject type: Invertebrate; Subject species: Caenorhabditis elegans (Factor headings shown in green)

mb_sample_id local_sample_id set batch genotype
SA200948aos142_ga_ms2_71 1 CB4856
SA200949aos145_ga_ms2_81 1 CB4856
SA200950aos127_ga_ms2_51 1 CX11314
SA200951aos76_ga_ms2_211 1 CX11314
SA200952aos25_ga_ms2_101 1 CX11314
SA200953aos46_ga_ms2_141 1 DL238
SA200954aos65_ga_ms2_191 1 DL238
SA200955aos50_ga_ms2_161 1 DL238
SA200956aos67_ga_ms2_201 1 N2
SA200957aos48_ga_ms2_151 1 N2
SA200958aos58_ga_ms2_181 1 N2
SA200959aos43_ga_ms4_131 1 PD1074
SA200960aos27_ga_ms3_111 1 PD1074
SA200961aos129_ga_ms2_61 1 PD1074
SA200962aos149_ga_ms2_91 1 PD1074
SA200963aos78_ga_ms4_221 1 PD1074
SA200964aos32_ga_ms2_121 1 RB2011
SA200965aos122_ga_ms2_41 1 RB2011
SA200966solera_31 1 solera
SA200967aos170_ga_ms2_321 2 CB4856
SA200968aos115_gt_ms1_291 2 CB4856
SA200969aos199_ga_ms2_381 2 CX11314
SA200970aos175_ga_ms2_351 2 CX11314
SA200971aos127_ga_ms3_241 2 CX11314
SA200972aos165_ga_ms2_301 2 DL238
SA200973aos192_ga_ms2_371 2 DL238
SA200974aos174_ga_ms2_341 2 DL238
SA200975aos106_co_ms2_251 2 N2
SA200976aos56_ga_ms2_411 2 N2
SA200977aos113_ga_ms1_281 2 PD1074
SA200978aos188_ga_ms3_361 2 PD1074
SA200979aos99_ga_ms2_261 2 PD1074
SA200980aos53_ga_ms2_401 2 PD1074
SA200981aos200_ga_ms2_391 2 PD1074
SA200982aos167_ga_ms3_311 2 PD1074
SA200985pooled_natural_isolate_421 2 pooled_natural_isolate
SA200986pooled_pd1074_431 2 pooled_pd1074
SA200983aos173_ga_ms2_331 2 RB2011
SA200984aos108_ga_ms2_271 2 RB2011
SA200987solera_441 2 solera
SA200988aos86_ga_ms2_652 3 KJ550
SA200989aos28_ga_ms2_532 3 KJ550
SA200990aos69_ga_ms1_642 3 PD1074
SA200991aos43_ga_bku_602 3 PD1074
SA200992aos90_ga_ms3_662 3 PD1074
SA200993aos27_ga_ms4_522 3 PD1074
SA200994aos99_ga_ms2_682 3 PD1074
SA200995aos38_ga_ms2_572 3 PD1074
SA200996aos185_ga_ms2_512 3 PD1074
SA200997aos37_ga_ms2_562 3 RB2347
SA200998aos74_ga_ms2_632 3 RB2347
SA200999aos36_ga_ms2_552 3 RB2347
SA201000aos35_ga_ms2_542 3 RB2550
SA201001aos40_ga_ms2_582 3 RB2550
SA201002aos71_ga_ms2_622 3 RB2550
SA201006solera_492 3 solera
SA201003aos98_ga_ms2_672 3 VC1265
SA201004aos42_ga_ms2_592 3 VC1265
SA201005aos184_ga_ms2_502 3 VC1265
SA201007aos109_ga_ms2_812 4 KJ550
SA201008aos100_ga_ms2_732 4 KJ550
SA201009aos134_ga_ms2_862 4 KJ550
SA201010aos140_ga_ms3_872 4 PD1074
SA201011aos113_ga_ms1_842 4 PD1074
SA201012aos180_ga_ms2_892 4 PD1074
SA201013aos92_ga_ms2_772 4 PD1074
SA201014aos87_co_ms3_722 4 PD1074
SA201015aos107_ga_bku_802 4 PD1074
SA201027pooled_mutant_902 4 pooled_mutant
SA201028pooled_pd1074_912 4 pooled_pd1074
SA201016aos95_ga_ms2_792 4 RB2347
SA201017aos116_ga_ms2_832 4 RB2347
SA201018aos171_ga_ms2_882 4 RB2347
SA201019aos82_ga_ms2_752 4 RB2347
SA201020aos81_ga_ms2_712 4 RB2550
SA201021aos111_ga_ms2_822 4 RB2550
SA201022aos96_ga_ms2_742 4 RB2550
SA201029solera_922 4 solera
SA201023aos84_ga_ms2_762 4 VC1265
SA201024aos73_ga_ms2_702 4 VC1265
SA201025aos125_ga_ms2_852 4 VC1265
SA201026aos93_ga_ms2_782 4 VC1265
SA201030aos79_ga_ms2_1163 5 AUM2073
SA201031aos51_ga_ms2_1093 5 AUM2073
SA201032aos91_ga_ms2_1193 5 AUM2073
SA201033aos75_ga_ms4_1153 5 PD1074
SA201034aos41_ga_ms2_1043 5 PD1074
SA201035aos44_ga_ms2_1063 5 PD1074
SA201036aos69_ga_ms3_1143 5 PD1074
SA201037aos87_ga_ms3_1183 5 PD1074
SA201038aos196_ga_ms2_1013 5 PD1074
SA201039aos181_ga_ms2_993 5 PD1074
SA201040aos83_ga_ms2_1173 5 RB2055
SA201041aos26_ga_ms2_1023 5 RB2055
SA201042aos45_ga_ms2_1103 5 RB2055
SA201051solera_973 5 solera
SA201043aos39_ga_ms2_1033 5 UGT49
SA201044aos49_ga_ms2_1083 5 UGT49
SA201045aos66_ga_ms2_1123 5 UGT60
SA201046aos33_ga_ms2_1053 5 UGT60
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Collection:

Collection ID:CO002172
Collection Summary:Escherichia coli (E. coli) IBAT (iterative batch average method) reference material and food source used throughout this experiment. Briefly, for each biological sample, a large-scale culture plate (LSCP) was used to generate a large mixed-stage population of worms (four to seven LSCP replicates per test strain). For each LSCP, worms were collected, population size estimated, and subsequently divided into at least 12 identical aliquots of 200,000 worms in ddH2O and flash-frozen in liquid nitrogen and stored at -80°C. As a quality control sample, C. elegans IBAT reference material was generated and saved in 200,000 worm aliquots.
Sample Type:Worms
Volumeoramount Collected:200,000 worms
Storage Conditions:-80℃

Treatment:

Treatment ID:TR002191
Treatment Summary:No treatments.

Sample Preparation:

Sampleprep ID:SP002185
Sampleprep Summary:Frozen lyophilized C. elegans aliquots were retrieved from -80°C. 200 μL of 1 mm zirconia beads were added to each sample and homogenized at 420 rcf for 90 seconds in a FastPrep-96 homogenizer and subsequently placed on dry ice for 90 seconds to avoid overheating, this step was repeated twice for a total of three rounds. Using the homogenized samples, 1 mL of 100% IPA chilled to -20°C was added to the lyophilized/homogenized sample powder and Zirconia beads in two increments of 500 μL. After each addition of 500 μL, samples were vortexed for 30 seconds – 1 minute and left at RT for 15 - 20 minutes. After RT incubation, samples were stored overnight (~12 hours) at -20°C. Samples were centrifuged for 30 minutes at 4°C (20,800 rcf). The supernatant was transferred to a new tube to use for analysis of non-polar molecules. 1 mL of pre-chilled 80:20 MeOH:H2O (4°C) was added to the remaining worm pellet to analyze polar molecules. The polar fraction shook at 4°C for 30 minutes. Samples were centrifuged at 20,800 rcf for 30 minutes at 4°C. The supernatant was transferred to a new tube to use for analysis of non-polar molecules. Both polar and non-polar samples were placed in a Labconco Centrivap at RT and monitored until completely dry. Once dry, polar and non-polar samples were reconstituted in D2O (99%, Cambridge Isotope Laboratories, Inc.) in a buffered solution with DSS (D6) and CDCl3 (99.96%, Cambridge Isotope Laboratories, Inc.) respectively. Samples were vortexed until fully soluble, and 45 μL of each sample were transferred into 1.7 mm NMR tubes (Bruker SampleJet) for acquisition.
Processing Storage Conditions:-80℃
Extraction Method:Sequential extraction of (1) IPA for non-polar molecule followed by (2) 80/20 MeOH/H2O for polar
Extract Storage:-80℃
Sample Resuspension:CDCl3 for non-polar; D2O (99%, Cambridge Isotope Laboratories, Inc.) in a buffered solution with DSS (D6) for polar

Analysis:

Analysis ID:AN003423
Laboratory Name:Edison Lab – Complex Carbohydrate Research Center
Analysis Type:NMR
Acquisition Date:2020-03-19
Operator Name:Amanda O. Shaver
Detector Type:Bruker Neo 1.7 mm TCI Cryo Probe
Data Format:ft
Num Factors:46
Num Metabolites:16
Units:Meta-Analysis Effect Size

NMR:

NMR ID:NM000232
Analysis ID:AN003423
Instrument Name:Bruker Neo 800 MHz
Instrument Type:FT-NMR
NMR Experiment Type:1D-1H
Spectrometer Frequency:800
NMR Probe:1.7 mm TCI cryoprobe
NMR Solvent:D2O
NMR Tube Size:1.7 mm
Shimming Method:Automatic (“Topshim”)
Pulse Sequence:noesypr1d
Water Suppression:3758.64 @ 4.7 ppm
Receiver Gain:65.1
Temperature:6
Number Of Scans:128
Dummy Scans:2
Acquisition Time:1.31 sec
Spectral Width:15
Num Data Points Acquired:32,768
Line Broadening:1.5
Apodization:exponential
Baseline Correction Method:Polynomial Automatic fit
Chemical Shift Ref Std:0.00
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