We focus on population-wide omics datasets. By curating these existing datasets, we can ensure the development of robust computational models.
- Genotype: Whole genome sequencing (>10 M SNPs)
- Raw sequencing data (Bukowski et al., 2018)
- Row VCF file on HCC:
path?
- AGPV5 genome filtration MAF < 0.05 and MR > 0.6:
vcf
- AGPV5 genome filtration MAF < 0.05 and MR > 0.6:
- Randomly sampled 50k SNPs
- GitHub Path:
data/01Genotype/282_agpv5_50.recode.vcf
data/01Genotype/282_agpv5_50k.txt
- GitHub Path:
- RNA-seq
- RNA-seq in seven tissues: CyVerse (Kremling et al., 2018)
- Root RNA-seq?
- Raw data?
- Process version?
- Microbiome
- Under high N and low N conditions (n=230 gentoypes x 2 N x 2 reps) (Meier et al., 2022)
- Root exudates
- Collected using GC-MS method?
- Metabolomics
- From seedling tissue with three replications (Z. Yang et al., 2022)
- Aboveground phenotypes
- More than 50 traits BLUP values
data/03Phenotype/MAP/public_pheno_282_37traits.xlsx
data/03Phenotype/MAP/public_pheno_282_mineral_ziegler.xlxs
- Six ear-related traits under different N conditions
- More than 50 traits BLUP values
- Belowground Phenotypes
- NA
Some big data were stored at OneDrive.
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- label corrected fq files
HCC: /work/jyanglab/SAP_raw_fq/
- label corrected fq files
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- Whole genome resequencing (WGS) data (Boatwright et al., 2022)
- 44 milion variants including 38 million SNPs, 5 million indels and 0.17 million CNVs
- Filteration: biallelic SNP, minor allele frequency (maf) > 0.05, missing data < 0.3, ite heterozygosity < 0.1
- Raw and filtered data on HCC Path
HCC: /common/schnablelab/hongyujin/SAPsnp/SNPallchrs/
- see filteration details:
profiling/SAP_SNPfilteration/preprocessSNP.sh
- see filteration details:
- Tunable genotyping by sequencing (tGBS) ~350 lines (Miao et al., 2020)
- Data on Figshare
- Whole genome resequencing (WGS) data (Boatwright et al., 2022)
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- In field agronomic traits
- github path
data/03Phenotype/SAP/
- 2020 SAP Schnable lab (Sorghum Asscoiation panel):
- The 2020 field experiment was planted on June 8. Experimental plot consisted of one 1.52-m row of plants from a single genotype planted with a spacing of 0.76 m between parallel and sequential rows and approximately 7.62 cm in spacing between sequential plants in the same row. No supplemental nitrogen was applied to low-nitrogen treatment blocks, and a target of 80 pounds of N per acre (89.7 kilograms/hectare) was applied to sufficient nitrogen blocks. The 2020 experiment was conducted in a field located at N°40.861, W°96.598. The 2020 experiment consisted of 347 genotypes drawn from the sorghum association panel plus Tx430. A total of four blocks were planted, each consisting of 390 plots with one entry per genotype, plus BTx623 as a repeated check. Two blocks were grown under HN treatment and two under LN treatment.
- 2021 SbDiv Schnable lab (Sorghum Diversity Panel)
- The 2021 field experiment was planted on May 25. Experimental plot consisted of one 1.52-m row of plants from a single genotype planted with a spacing of 0.76 m between parallel and sequential rows and approximately 7.62 cm in spacing between sequential plants in the same row. No supplemental nitrogen was applied to low-nitrogen treatment blocks, and a target of 80 pounds of N per acre (89.7 kilograms/hectare) was applied to sufficient nitrogen blocks. The 2021 experiment was conducted in a field located at N°40.858, W°96.596. The 2021 experiment consisted of 347 genotypes replicated in two blocks, each consisting of 390 plots including the replicated check, under LN conditions as in 2020 and 911 sorghum genotypes in two blocks, each consisting of 966 plots including the replicated check under HN. The larger population in HN treatment resulted from the inclusion of sorghum genotypes from the sorghum diversity panel in addition to the previously characterized sorghum association panel (SAP) lines.
- 2023 SAP Chlorophyll (by Luyang Zhang)
- github path
- Greenhouse seedling phenotype
- 346 lines HN and LH
- Leaf number, plant height, root and shoot fresh weight, photosynthesis traits (LICOR-600), chorophyll (large missing rate)
- 346 lines HN and LH
- Panicle phenotype
- Kyle Linders thesis?
- Nathan
- In field agronomic traits
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- Files with RNA-Seq-based markers called through GATK and gene expression normalized as Transcripts per million (TPM) are deposited at OneDrive.
- Measurements of plant traits and tissue samples for gene expression were collected from a field experiment conducted at the University of Nebraska-Lincoln Havelock Research Farm in Lincoln, NE (40.859, -96.597) in 2021. The field consisted of a total of 1,936 plots split into two blocks of 968 plots. Each block included single entries of 915 genotypes, four extra replications of TX430, and 51 plots of BTx623 as a replicated check. Each plot consistent of a 5 foot rows of plants, 2.5 alleyways, target spacing of 3 inches between plants, and 30 inch (approximately 0.75 meter) spacing between parallel and sequential rows. The field was treated with anhydrous ammonia fertilizer at a target rate of rate of 80 pounds of N per acre (approximately 89 kilograms per hectare). Planting occurred on May 25th, 2021.
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Leaf tissue samples were collected on August 5th, 2021, with sampling beginning at 10:00am and ending at 12:00noon. For each plot, a single representative plant was selected for sampling, avoiding edge plants where possible. Samples were collected from the fourth leaf, counting downwards from the uppermost fully expanded leaf, or the flag leaf, if present. Leaf tissue samples were immediately flash frozen in liquid nitrogen and then transferred to dry ice for transport. Leaf tissue samples were continuously stored either in -80 freezers or on dry ice until RNA extraction commenced.
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To guide group members having a better sense about the project layout, here we briefly introduce the specific purposes of the dir system. The layout of dirs is based on the idea borrowed from ProjectTemplate.
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The guideline for the collaborative workflow.
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Check out progress and things to-do and throw ideas via the wiki page.
This is an ongoing research project. It was intended for internal lab usage. It has not been extensively tested. Use at your own risk. It is a free and open source software, licensed under GPLv3.