Kim, Kwanho · Lin, Zechuan · Simmons, Sean · et al.

1 files · 37 KB · pdf

This dataset contains CCS corrected HiFi long-read DNA sequencing (lrDNAseq) in FASTQ format for 100 PMDBS samples from Parkinson's patients and healthy controls. It's part of the PD5D atlas, where the same subjects were also profiled with other omics assays including genotyping, single-cell ATACseq, and spatial transcriptomics.

Kim, Kwanho · Lin, Zechuan · Simmons, Sean · et al.

1 files · 37 KB · pdf

This dataset contains raw FASTQ files from the midbrain single-nucleus RNA sequencing (snRNAseq) dataset with hybrid selection for the matching PMDBS samples from the PD5D chort. The same subjects were also profiled with other omics assays including genomic DNAseq, genotyping, single-cell ATACseq, and spatial transcriptomics.

Pančíková, Alexandra · Theunis, Koen · Hulselmans, Gert · et al.

1 files · 37 KB · pdf

This dataset consists of raw sequencing snRNA-seq data (10x Genomics Chromium Next GEM Single Cell 3ʹ). The data is part of an overall set of samples derived from postmortem midbrain (n=140), cingulate cortex (n=190) and motor cortex (n=4) of healthy donors (n=114), patients with Parkinson's disease (n=75) or patients with other neurological disorder (n=1). The protocol followed to isolate nuclei from postmortem brain samples and to prepare sequencing libraries can be found below. To increase throughput and to decrease batch effects, several donors have been pooled together into a single sequencing library. To computationally demultiplex the nuclei to their corresponding donors, cellsnp-lite (version commit: aad18644adcde853c313362a856a24245c9b91f7) followed by vireo (https://github.com/single-cell-genetics/vireo/pull/108) has been used. The population VCF with the donor genotypes derived from whole genome sequencing data has been used to assign nuclei back to their donors.

Pančíková, Alexandra · Theunis, Koen · Hulselmans, Gert · et al.

1 files · 36 KB · pdf

This dataset consists of raw sequencing snRNA-seq data using ParseBio Evercode Whole Transcriptome. The data is part of an overall set of samples derived from postmortem midbrain (n=140), cingulate cortex (n=190) and motor cortex (n=4) of healthy donors (n=114), patients with Parkinson's disease (n=75) or patients with other neurological disorder (n=1). The protocol followed to isolate nuclei from postmortem brain samples and to prepare sequencing libraries can be found below. To increase throughput and to decrease batch effects, several donors have been pooled together into a specific ParseBio barcode. To computationally demultiplex the nuclei to their corresponding donors, cellsnp-lite (version commit: aad18644adcde853c313362a856a24245c9b91f7) followed by vireo (https://github.com/single-cell-genetics/vireo/pull/108) has been used. The population VCF with the donor genotypes derived from whole genome sequencing data has been used to assign nuclei back to their donors.

Pančíková, Alexandra · Theunis, Koen · Hulselmans, Gert · et al.

1 files · 36 KB · pdf

This dataset consists of raw sequencing snATAC-seq data (10x Genomics Chromium Next GEM Single Cell ATAC v2). The data is part of an overall set of samples derived from postmortem midbrain (n=140), cingulate cortex (n=190) and motor cortex (n=4) of healthy donors (n=114), patients with Parkinson's disease (n=75) or patients with other neurological disorder (n=1). The protocol followed to isolate nuclei from postmortem brain samples and to prepare sequencing libraries can be found below. To increase throughput and to decrease batch effects, several donors have been pooled together into a single sequencing library. To computationally demultiplex the nuclei to their corresponding donors, cellsnp-lite (version commit: aad18644adcde853c313362a856a24245c9b91f7) followed by vireo (https://github.com/single-cell-genetics/vireo/pull/108) has been used. The population VCF with the donor genotypes derived from whole genome sequencing data has been used to assign nuclei back to their donors. (edited)

Pančíková, Alexandra · Theunis, Koen · Hulselmans, Gert · et al.

1 files · 36 KB · pdf

This dataset consists of raw sequencing snATAC-seq data (HyDrop v2). The data is part of an overall set of samples derived from postmortem midbrain (n=140), cingulate cortex (n=190) and motor cortex (n=4) of healthy donors (n=114), patients with Parkinson's disease (n=75) or patients with other neurological disorder (n=1). The protocol followed to isolate nuclei from postmortem brain samples can be found below. To increase throughput and to decrease batch effects, several donors have been pooled together into a single sequencing library. To computationally demultiplex the nuclei to their corresponding donors, cellsnp-lite (version commit: aad18644adcde853c313362a856a24245c9b91f7) followed by vireo (https://github.com/single-cell-genetics/vireo/pull/108) has been used. The population VCF with the donor genotypes derived from whole genome sequencing data has been used to assign nuclei back to their donors.

Pančíková, Alexandra · Theunis, Koen · Hulselmans, Gert · et al.

1 files · 36 KB · pdf

This dataset consists of raw sequencing ATAC-seq data (Scale-ATAC pre-indexing followed by 10x Genomics snATAC v2). The data is part of an overall set of samples derived from postmortem midbrain (n=140), cingulate cortex (n=190) and motor cortex (n=4) of healthy donors (n=114), patients with Parkinson's disease (n=75) or patients with other neurological disorder (n=1). The protocol followed to isolate nuclei from postmortem brain samples and to prepare sequencing libraries can be found below. To increase throughput and to decrease batch effects, several donors have been pooled together into a single sequencing library. To computationally demultiplex the nuclei to their corresponding donors, cellsnp-lite (version commit: aad18644adcde853c313362a856a24245c9b91f7) followed by vireo (https://github.com/single-cell-genetics/vireo/pull/108) has been used. The population VCF with the donor genotypes derived from whole genome sequencing data has been used to assign nuclei back to their donors.

Pančíková, Alexandra · Theunis, Koen · Hulselmans, Gert · et al.

1 files · 36 KB · pdf

This dataset consists of raw sequencing ATAC-seq data (Scale-ATAC + HyDrop v2). The data is part of an overall set of samples derived from postmortem midbrain (n=140), cingulate cortex (n=190) and motor cortex (n=4) of healthy donors (n=114), patients with Parkinson's disease (n=75) or patients with other neurological disorder (n=1). The protocols followed to isolate nuclei from postmortem brain samples and to prepare sequencing libraries can be found below. To increase throughput and to decrease batch effects, several donors have been pooled together into a single sequencing library. To computationally demultiplex the nuclei to their corresponding donors, cellsnp-lite (version commit: aad18644adcde853c313362a856a24245c9b91f7) followed by vireo (https://github.com/single-cell-genetics/vireo/pull/108 ) has been used. The population VCF with the donor genotypes derived from whole genome sequencing data has been used to assign nuclei back to their donors.

Pančíková, Alexandra · Theunis, Koen · Hulselmans, Gert · et al.

1 files · 37 KB · pdf

This dataset consists of raw sequencing snRNA-seq data and snATAC-seq data (10x Genomics Chromium Next GEM Multiome ATAC/GEX). The data is part of an overall set of samples derived from postmortem midbrain (n=140), cingulate cortex (n=190) and motor cortex (n=4) of healthy donors (n=114), patients with Parkinson's disease (n=75) or patients with other neurological disorder (n=1). The protocol followed to isolate nuclei from postmortem brain samples and to prepare sequencing libraries can be found below. To increase throughput and to decrease batch effects, several donors have been pooled together into a single sequencing library. To computationally demultiplex the nuclei to their corresponding donors, cellsnp-lite (version commit: aad18644adcde853c313362a856a24245c9b91f7) followed by vireo (https://github.com/single-cell-genetics/vireo/pull/108 ) has been used. The population VCF with the donor genotypes derived from whole genome sequencing data has been used to assign nuclei back to their donors. (edited)

Yuan, Guangyuan

72 rows × 13 cols · 6.0 KB · csv, fasta

11 numeric · 2 categorical

This dataset supports the findings of the manuscript "Root anatomical traits modulate the assembly and nitrogen transformation potential of root-associated microbiomes in a temperate steppe" (NPH-MS-2026-55667). It contains root traits data, bacterial 16S rRNA gene absolute abundances, functional genes relative abundances, DNA extraction metadata, and phylogenetic marker sequences for 37 plant species from a temperate steppe ecosystem. The dataset includes the following files: 1. root traits.csv - Root traits including average diameter (AD), specific root length (SRL), specific root area (SRA), root tissue density (RTD), root nitrogen content (RNC), root carbon content (RCC), carbon‑nitrogen ratio (RCN), cortex layer number (CLN), cortex thickness (CT), and the ratio of cortex thickness to root diameter (CTRD). The first column lists plant species names. 2. Absolute abundance of 16S rRNA gene.csv - Quantitative PCR (qPCR) derived absolute abundances of bacterial 16S rRNA gene copies (copies/ng DNA) across different root compartments (rhizosphere, rhizoplane, endosphere), host species, root orders, and cotyledon classes (monocot/dicot). 3. DNA extraction sample weight.csv - Fresh weight (grams) of root material used for DNA extraction for each sample, linked by SampleID to the abundance data. 4. DNA extraction concentration.csv - Qubit‑measured DNA concentrations (ng/μL) and the sample volume (μL) used for quality control, together with sample metadata. 5. 37species.fasta - DNA sequences of two chloroplast markers (matK and rbcL) for the 37 plant species included in the study. The sequences are in FASTA format with headers formatted as ">Species". These were used for host phylogeny construction and Pagel's λ analyses. 6. Quantitative PCR results of functional gene.csv - Quantitative PCR (qPCR) derived relative abundances of bacterial 16S rRNA gene and functional genes across different root compartments (rhizosphere, rhizoplane, endosphere), host species, root orders, and cotyledon classes (monocot/dicot). 7. README.md - A detailed description of each file, column headers, abbreviations, units, and any missing value codings (NA). All data are provided to ensure transparency and reproducibility of the analyses. For methodological details, please refer to the Materials and Methods section of the associated publication. These data are under embargo until the associated research article is published. After that date, they will be freely available under a Creative Commons Attribution 4.0 International (CC BY 4.0) license. During the embargo period, the metadata (title, authors, abstract) and the DOI remain publicly visible, but the data files are not accessible. For access requests before the embargo expires, please contact the corresponding author.

MacDonald, Adam · Stratton, Jo Anne

1 files · 35 KB · pdf

We performed 10X Genomics single-cell RNAsequencing of human prepheral blood mononuclear cells from healthy control, PD and RBD patients. This dataset contains raw FASTQ files. Sequencing was performed using NovaSeq 6000 S4 PE 100bp. Reads were processed using the 10X Genomics Cell Ranger Single Cell 2.0.0 pipeline. FASTQs generated from sequencing output were aligned to the human GRCh38 reference genome using STAR algorithm 2.7.3a.

Stratton, Jo Anne · Mukherjee, Sriparna · Trudeau, Louis-Eric

1 files · 5.0 KB · pdf

We performed bulk RNAsequencing of substantia nigra from wild type and PINK1 KO mice 26-days post C.rodentium infection. This dataset contains raw fastq files from striatal cells, sorted into 4 groups namely wild type and PINK1 KO uninfected and infected mice. Sequencing was performed using NextSeq500. FASTQs generated from sequencing output were aligned to the mm10 reference genome using STAR aligner.

Stratton, Jo Anne · Mukherjee, Sriparna · Trudeau, Louis-Eric

1 files · 6.1 KB · pdf

We performed bulk RNAsequencing of striatum from wild type and PINK1 KO mice 26-days post C.rodentium infection. This dataset contains raw fastq files from striatal cells, sorted into 4 groups namely wild type and PINK1 KO uninfected and infected mice. Sequencing was performed using NextSeq500. FASTQs generated from sequencing output were aligned to the mm10 reference genome using STAR aligner.

Recinto, Sherilyn · Stratton, Jo Anne

1 files · 6.1 KB · pdf

We performed 10X Genomics single-cell RNAsequencing of human iSPC-derived monocytes and macrophages in vitro. Cells were treated with 500 ng/mL lipopolysaccharide (LPS) and 50 ng/mL interleukin-1 beta (IL1b) for 24 hours. This dataset contains raw FASTQ files from myeloid cells, sorted into 4 groups namely monocytes (Mono) and Macrophages (Mac) non-stimulated (NS) and LPS+IL1b-stimulated cells. Sequencing was performed using NovaSeq 6000 S4 PE 100bp. Reads were processed using the 10X Genomics Cell Ranger Single Cell 2.0.0 pipeline. FASTQs generated from sequencing output were aligned to the human GRCh38 reference genome using STAR algorithm 2.7.3a.

Recinto, Sherilyn · Stratton, Jo Anne · Pei, Jessica · et al.

2 files · 6.0 KB · pdf

We performed 10X Genomics single-cell RNAsequencing of colonic lamina propria cells from wild type and LRRK2 G2019S mice following 1-week post C. rodentium infection. The cells were pooled from 3 mice per group of both sexes at 8-12 weeks of age. This dataset contains raw FASTQ files from mouse colonic lamina propria, sorted into 4 groups namely wild type and LRRK2 G2019S uninfected and infected mice. Sequencing was performed using NovaSeq 6000 S4 PE 100bp. Reads were processed using the 10X Genomics Cell Ranger Single Cell 2.0.0 pipeline. FASTQs generated from sequencing output were aligned to the mouse GRCm38 reference genome using STAR algorithm 2.7.3a.

Recinto, Sherilyn · Stratton, Jo Anne

1 files · 5.7 KB · pdf

We performed 10X Genomics single-cell RNA sequencing of colonic lamina propria cells from wild type and PINK1 KO mice following either 1-week or 2-weeks post C. rodentium infection. The cells were pooled from 3 mice per group of both sexes at 8-12 weeks of age. This dataset contains raw FASTQ files from mouse colonic lamina propria, sorted into 8 groups namely wild type and PINK1 KO uninfected and infected mice at 1- or 2-weeks post-infection. Sequencing was performed using NovaSeq 6000 S4 PE 100bp. Reads were processed using the 10X Genomics Cell Ranger Single Cell 2.0.0 pipeline. FASTQs generated from sequencing output were aligned to the mouse GRCm38 reference genome using STAR algorithm 2.7.3a.

Budzinski, Lisa · Beenken, Anne Elisabeth · Sempert, Toni · et al.

9 rows × 1 cols · 743 B · csv, docx, zip

1 categorical

We have investigated an IgG4-RD (IgG4-RD) cohort by our multi-parameter microbiota flow cytometry approach to characterise the microbiota on single-cell level for attributes of the disease. The microbiota is isolated from stool samples and stained according to the published protocol for (a) host immunoglobulins IgA1, IgA2, IgM, IgG and (b) agglutinin binding to mannose, galactose or N-Acetyl-glucosamine surface sugar moieties. For all samples we also determined the microbiome composition by 16S rRNA (V3-V4) sequencing on the illumina MiSeq platform. We provide the raw .fcs and FASTQ files of 40 IgG4-RD patients. For comparison we additionally analysed 36 healthy donors. All .fcs files were generated on BD Influx®. The metadata is collected in the provided meta.csv. The staining parameters are summarized in provided panel.csv.

Gómez Maqueo Anaya, Sofía · Dos Santos Souza, Eduardo José · Fomba, Khanneh Wadinga · et al.

116 rows × 16 cols · 7.0 KB · csv

11 categorical · 5 numeric

The dataset consists of three files: In-situ-NorthAfrica-compilation.csv : This file contains a compilation of in situ datasets used to produce the initial scatterplots comparing modeled and measured mineral mass fractions. All values are given as mass fraction percentages (%). The first column lists the authors associated with each published measurement. Elemental_CM-DUSTRISK-Praia.csv : This file includes the updated elemental mass concentration measurements used for comparison against the DUSTRISK2022 dataset. Measured total mass is reported in μg/m³, while elemental concentrations are given in ng/m³. The COSMO-MUSCAT outputs are identified by the prefix "CM" and are reported in μg/m³. "SD" denotes standard deviation. All variables ending in "_frac" represent mass fraction percentages (%). measurements_and-CM_compilation-JATAC2022.csv : This file contains measured elemental and the updated mineral mass fractions used for the results presented in the subsections 5.1.2 "Comparison with JATAC 2022" and 5.2.1 "JATAC 2022" . Particle size classes correspond to the MUSCAT size bins (see Table 1 of the associated manuscript) and are provided in separate columns following the format "X##", where X denotes the mineral or element and ## corresponds to MUSCAT bins (i.e., 01, 03, 09, or 26). Modeled values are provided in columns starting with "CM". The prefixes "CI025" and "CI975" denote the lower and upper confidence intervals, respectively.

Zamora, Esteban · Perez de Lara, David · Guidi, Luca · et al.

164 rows × 70 cols · 94 KB · csv, xlsx

70 numeric

Dataset corresponding to the figures of the article: Esteban Zamora-Amo, et al. "Ultra-Conformal memristors for on-skin electronics".