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Citations for Illumina :
1 - 50 of 796 citations for Peripheral Blood Mononuclear Cell since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Genomics 2020Quote: DNA methylation was assessed genome-wide from peripheral blood with commercial arrays from Illumina (CA, USA). The Infinium MethylationEPIC BeadChip ...
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bioRxiv - Genomics 2020Quote: Peripheral blood DNA genotypes were obtained for 238 subjects using Infinium Multi-Ethnic Global-8 Kit (Illumina, San Diego, CA) and processed with GenomeStudio software ...
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bioRxiv - Genetics 2023Quote: ... Plasma was divided from maternal peripheral blood (5[mL) by centrifuging and then 600[μL (Ion Torrent) or 1.4 mL (Illumina CN500) plasma was used to extract cell-free DNA ...
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bioRxiv - Cancer Biology 2020Quote: ... the genomic DNA extracted from whole mononuclear cells from fresh BM aspirates underwent amplicon-based targeted NGS analysis on a MiSeq sequencer (Illumina Inc., San Diego, CA, USA), as described previously52 ...
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bioRxiv - Genomics 2022Quote: Blood DNA methylation profiles (Illumina 450k array) from six groups of monozygotic twin pairs were analysed.
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bioRxiv - Genomics 2020Quote: ... CNV analysis was performed on a combined cohort of 130 sequenced hESC lines and a control cohort consisting of 243 human samples from primary blood or lymphoblastoid cell lines (LCL) that had undergone WGS on the same platform (Illumina HiSeqX) and to similar depth as the hESC lines (Pato et al. ...
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bioRxiv - Genetics 2022Quote: Blood DNAm was profiled using the Infinium MethylationEPIC BeadChip (Illumina Inc.) in two sample sets from GS ...
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bioRxiv - Genomics 2022Quote: ... The current study involved measurement of blood DNA methylation by Illumina Methylation EPIC Bead Chips (EPIC array ...
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bioRxiv - Genetics 2022Quote: Blood DNAm was profiled using the same Infinium MethylationEPIC BeadChip (Illumina Inc.) as used by GS ...
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bioRxiv - Genomics 2023Quote: ... this filter step used both germline blood sequencing and standard fidelity (Illumina) tumor sequencing to focus the analysis on low-level mosaic calls.
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bioRxiv - Genomics 2024Quote: Whole blood DNA methylation was profiled using the Infinium MethylationEPIC BeadChip (Illumina Inc.) in two sets of GS participants at two separate times by the Wellcome Trust Clinical Research Facility ...
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bioRxiv - Microbiology 2020Quote: ... RNA was rRNA depleted with Ribo-Zero ScriptSeq Complete Gold (Blood) (Illumina, San Diego, CA) and sequencing libraries were constructed using the TruSeq Stranded Total RNA kit (Illumina) ...
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bioRxiv - Immunology 2019Quote: ... cDNA for whole-blood was prepared using the TruSeq Stranded mRNA kit (Illumina, CA, USA). Libraries were amplified and then sequenced on an Illumina NextSeq (2 × 75 ...
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bioRxiv - Genetics 2023Quote: ... DNA was extracted from whole blood using MasterPure DNA Purification Kit (Biozym, Illumina Inc, USA). DNA quality and quantity estimation was done by agarose gel electrophoresis and spectrophotometry ...
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bioRxiv - Genomics 2023Quote: ... variant calls were used in this step from both germline blood sequencing and standard fidelity (Illumina) tumor sequencing to focus the analysis on low-level mosaic calls.
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bioRxiv - Genetics 2023Quote: ... Libraries from blood samples were sequenced as paired end 100bp reads on an Illumina NovaSeq6000 (Illumina), whereas libraries from cerebellum samples were sequenced as paired-end 68 bp reads on a HiSeq2000 (Illumina) ...
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bioRxiv - Molecular Biology 2024Quote: ... we used the 318 curated files containing raw human blood expression data (FASTQ containing Illumina reads) of the Bgee project (see supplementary data of (Bastian et al ...
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bioRxiv - Microbiology 2022Quote: Short read sequencing from blood culture broth extractions utilised the Nextera DNA Flex Library Prep Kit (Illumina), with a modification of the starting input of 5 μL gDNA with samples >20 ng/μL ...
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bioRxiv - Cancer Biology 2024Quote: ... P-BOs and NP-BOs and 30X target depth for matched normal (blood) was performed by Illumina, the Sanger Institute ...
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bioRxiv - Neuroscience 2020Quote: ... nDNA was extracted from whole blood and genotyped on Illumina GWAS arrays for ADNI1 (Illumina Human 610-Quad BeadChip), ADNI GO/2 participants (Illumina HumanOmniExpress BeadChip) ...
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bioRxiv - Cancer Biology 2021Quote: ... Tumor DNA was isolated using the Qiagen Blood and Tissue Kit and sgRNA cassette was amplified similarly to the in vitro screen and analyzed by Illumina sequencing ...
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bioRxiv - Microbiology 2020Quote: DNA were extracted by QIAGEN DNeasy Blood and Tissue Kit and sequencing libraries were prepared using the Nextera XT kit and sequenced on a MiSeq (Illumina) using v3 reagents with 2 × 300 cycles ...
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bioRxiv - Genetics 2021Quote: ... sequencing libraries were generated from whole blood-derived fragmented DNA using the TruSeq DNA Nano kit (Illumina, Inc., San Diego, USA) and sequence reads were generated using a HiSeq X Ten1 system (Illumina ...
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bioRxiv - Neuroscience 2019Quote: We used standard methods to extract genomic DNA from EDTA blood to perform genome-wide SNP (single nucleotide polymorphism) genotyping of all individuals using the Infinium PsychArray (Illumina Inc). Quality control and imputation was performed with Gimpute (31 ...
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bioRxiv - Neuroscience 2020Quote: ... Most PNC subjects were genotyped from blood samples on the 550HH and 610-Quad SNP arrays from Illumina (Illumina Inc., San Diego, CA). Analyses were performed using PLINK 1.9 (Chang et al. ...
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bioRxiv - Neuroscience 2020Quote: IMAGEN subjects were genotyped from blood samples on 610-Quad SNP and 660-Quad SNP arrays from Illumina (Illumina Inc., San Diego, CA). Most PNC subjects were genotyped from blood samples on the 550HH and 610-Quad SNP arrays from Illumina (Illumina Inc. ...
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bioRxiv - Genetics 2019Quote: DNA from subjects in the discovery cohort was extracted from either whole blood or saliva and genotyped using the Illumina 610k beadchip (Illumina, San Diego, CA). Standard GWAS QC was conducted at the samples and variants level ...
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bioRxiv - Genomics 2023Quote: ... and dizygotic (DZ) twin pairs who had completed the questionnaires regarding puberty (see below) and had blood DNA methylation data (Illumina 450K or EPIC) in early adulthood available.
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bioRxiv - Genomics 2023Quote: The FUSION cohort samples were genotyped using DNA extracted from blood on the HumanOmni2.5 4v1 H BeadChip array (Illumina, San Diego, CA, USA) during a previous study (Taylor et al. ...
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bioRxiv - Genetics 2020Quote: Blood samples of forty eight female GRF goats were collected and animals were genotyped with the Illumina GoatSNP50 BeadChip (Illumina Inc., San Diego, CA) containing 53,347 Single Nucleotide Polymorpishms (SNPs ...
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bioRxiv - Genetics 2019Quote: WGS was performed on DNA extracted from whole blood at 30x coverage using Illumina HiSeq X Ten system (Illumina, Inc., San Diego, CA, USA) with 150bp paired-end reads ...
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bioRxiv - Genomics 2021Quote: ... we generated whole genome sequences of the 139 subjects using DNA isolated from blood (130 subjects) or skin fibroblasts (nine subjects) on the HiSeq4000 (Illumina; 150 bp-paired end), SNVs and small indels were called using GATK 83 ...
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bioRxiv - Genetics 2020Quote: ... DNA was extracted from whole blood and genotyping was performed at the Wellcome Trust Sanger Institute (Hinxton, UK) on the Human670-QuadCustom Illumina BeadChip (Illumina, Inc., San Diego, CA, USA), as previously described (103–105) ...
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bioRxiv - Developmental Biology 2022Quote: ... SP flow cell (Illumina).
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bioRxiv - Microbiology 2019Quote: ... BV2 cells were then single cell cloned and G3BP1 was sequenced by Illumina HiSeq ...
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bioRxiv - Microbiology 2019Quote: ... BV-2 cells were then single cell cloned and G3BP1 was sequenced by Illumina HiSeq ...
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bioRxiv - Cell Biology 2023Quote: ... performed on 24 cells/cell line using a NextSeq 500 (Illumina, San Diego, CA). Data analysis was performed as described previously69 ...
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bioRxiv - Cancer Biology 2021Quote: ... or S4 flow cell (Illumina).
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bioRxiv - Molecular Biology 2021Quote: ... 300 cycles flow cell (Illumina), with the following parameters ...
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bioRxiv - Cancer Biology 2023Quote: ... or S4 flow cell (Illumina). The average number of read pairs per normal was 614 million and the average number of read pairs per tumor was 1.3 billion.
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bioRxiv - Cancer Biology 2021Quote: ... Single cell derived cDNA libraries were sequenced on NovaSeq S4 cell sequencer (Illumina, San Diego, CA). Cellranger (10x Genomics ...
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bioRxiv - Cancer Biology 2021Quote: ... cells were tagmented with TDE1 (Illumina) for 30 min at 37°C ...
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bioRxiv - Synthetic Biology 2019Quote: ... A MiSeq nano flow cell (Illumina) was clustered with a 4pM library comprised of 90% PhiX and 10% PCR-prepared library ...
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bioRxiv - Genetics 2020Quote: ... 100 cycles flow cell (Illumina Inc.). Amplified fragmented cDNA of 300 bp in size were sequenced in single-end mode with a read length of 100 bp ...
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bioRxiv - Cancer Biology 2021Quote: ... 2 × 150 bp flow cells (Illumina).
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bioRxiv - Cell Biology 2020Quote: ... loaded on a flow cell (Illumina) and sequenced on a NextSeq 500 platform (Illumina ...
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bioRxiv - Cell Biology 2020Quote: ... loaded on a flow cell (Illumina) and sequenced on a HiSeq 4000 platform (Illumina ...
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Human CCR6+ Th cells show both an extended stable gradient of Th17 activity and imprinted plasticitybioRxiv - Immunology 2023Quote: ... and analyzed using Cell Ranger (Illumina).
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bioRxiv - Developmental Biology 2024Quote: ... 150 cycles flow cells (Illumina, 20024907). Library preparations of one sample per genotype were run on a single flow cell ...
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bioRxiv - Cell Biology 2021Quote: ... Cells were submitted for 10x library preparation for 3’ single cell sequencing on a NovaSeq 6000 (Illumina) at the Cancer Research UK Cambridge Institute ...