Labshake search
Citations for Illumina :
3901 - 3950 of 10000+ citations for Creatinine Serum Low Sample Volume Kit 384 well Plate since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Microbiology 2019Quote: ... the three samples were also subjected to 16S rRNA gene amplicon sequencing on a MiSeq benchtop sequencer (Illumina Inc.). DNA was extracted from separate aliquots of the same sediment samples using the DNeasy PowerLyzer PowerSoil kit (MO BIO Laboratories ...
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bioRxiv - Molecular Biology 2019Quote: ... Raw data was de-multiplexed and FASTQ files for each sample was generated using the bcl2fastq software (Illumina inc.). FASTQ data were checked using the FastQC tool (http://www.bioinformatics.babraham.ac.uk/projects/fastqc/) ...
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bioRxiv - Plant Biology 2020Quote: ... Paired-end sequencing libraries (150bp × 2) were constructed for the HA and LA samples following manufacturer’s instructions (Illumina, USA). The libraries were sequenced in Illumina Genome Analyzer ×10 platform by NBT ...
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bioRxiv - Developmental Biology 2020Quote: ... Clean PCR amplicons from the same DNA sample were pooled to generate 137 libraries that were sequenced by Illumina MiSeq v3 ...
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bioRxiv - Microbiology 2021Quote: ... cDNA libraries containing pooled barcoded samples was run across two lanes of a HiSeq400 (Illumina, San Diego, CA, USA) on two separate runs for 150 bp paired-end reads (http://dnatech.genomecenter.ucdavis.edu/) ...
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bioRxiv - Genomics 2021Quote: ... Each sample library was uniquely barcoded and quantified by qPCR using a PhiX Control v3 (Illumina, FC-110-3001) standard curve ...
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bioRxiv - Genetics 2019Quote: ... and cDNA libraries were constructed following the protocol “Preparing samples for sequencing of mRNA” (Illumina Inc., San Diego, CA).
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bioRxiv - Genetics 2019Quote: ... All sequencing followed the protocol in the Illumina TruSeq PCR-Free Sample Preparation Guide (Illumina cat# FC-121-2001), and used PCR-free library preparation kits purchased from KAPA Biosystems (see https://www.nhlbiwgs.org/topmed-whole-genome-sequencing-project-freeze-5b-phases-1-and-2 for additional details) ...
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bioRxiv - Genetics 2020Quote: ... One microgram of total RNA was used for library preparation following the TruSeq Stranded mRNA Sample Preparation Protocol (Illumina). Sequencing was performed on an Illumina HiSeq 2000 platform at Wageningen University & Research ...
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bioRxiv - Cancer Biology 2020Quote: ... DNA methylation profiling of all samples was performed using the Infinium MethylationEPIC (850k) BeadChip (Illumina, San Diego, CA, USA) or Infinium HumanMethylation450 (450k ...
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bioRxiv - Cell Biology 2020Quote: Illumina libraries were prepared from between 0.5 and 10ng of amplified cDNA using the Nextera XT DNA sample preparation protocol (Illumina) and a 1:1 Ampure XP purification step was performed ...
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bioRxiv - Physiology 2021Quote: ... and sequenced to a total of 25 million reads per sample on a Novaseq platform (Illumina, San Diego, CA).
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bioRxiv - Neuroscience 2021Quote: The clustering of the index-coded samples was performed on a cBot Cluster Generation System (Cat.No. SY401-2015, Illumina) using TruSeq PE Cluster Kit v3-cBot-HS (Cat.No ...
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bioRxiv - Evolutionary Biology 2020Quote: ... and the samples were pair-end sequenced (Micro V2, 300 cycles) on a MiSeq equipment (Illumina, San Diego, USA) in around 18 hours ...
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bioRxiv - Neuroscience 2021Quote: ... Ribosomal RNA was depleted from the samples using TruSeq total RNA rRNA-depletion protocol (Illumina, Cat. #RS-122-2201) and then RNA samples were purified using Agencourt RNAClean XP beads (Beckman Coulter).
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bioRxiv - Microbiology 2021Quote: ... Sample libraries were pooled and diluted to 200pm and 100µl of this diluted sample was loaded onto a flow cell for NGS using an iSeq 100 (Illumina). Sequences were assembled using reference mapping with paired ends in Geneious R10 (Biomatters ...
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bioRxiv - Genomics 2021Quote: ... High quality samples were then sequenced to a minimum of 50,000 reads per cell on a NextSeq 500 sequencer (Illumina) using a 75-cycle High Output kit using a custom read1 primer (GCCTGTCCGCGGAAGCAGTGGTATCAACGCAGAGTAC).
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bioRxiv - Cell Biology 2020Quote: ... Samples were sequenced as 150bp paired end reads on multiplexed lanes of an Illumina HiSeq3000 (Illumina Inc, CA, USA). All sequencing data has been submitted to the European Nucleotide archive under the study accession PRJEB41493.
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bioRxiv - Molecular Biology 2022Quote: ... Sample libraries were sequenced on a HiSeq 2500 or a NextSeq 550 sequencing device (Illumina, San Diego, CA, USA) with a paired end read output of 2 × 250 bp (HiSeq ...
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bioRxiv - Cancer Biology 2022Quote: ... All libraries were sequenced with a depth of at least 50,000 reads per spot (minimum of ~250 millions per sample) at the NovaSeq (Illumina). The Visium Human Transcriptome Probe Set v1.0 contains probes to 19,144 genes and after computational preprocessing (filtering for probes off-target activity ...
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bioRxiv - Plant Biology 2022Quote: The triplicate total RNA samples used for single-end 1×75bp RNA-Seq on a NextSeq500 sequencing platform (Illumina). After examining the data quality using FastQC (v0.11.5) ...
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bioRxiv - Microbiology 2022Quote: ... Shotgun metagenomes were sequenced from the extracted samples on the Illumina NovaSeq 6000 (Illumina, San Diego, CA, United States), with a 150 bp paired-end sequencing strategy ...
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bioRxiv - Pathology 2022Quote: ... This library was sequenced with 43 other samples on a Hiseq3000 instrument (2×150 bp paired-end reads) (Illumina) at the GeT-PlaGe INRAE Sequencing facility (Toulouse ...
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bioRxiv - Neuroscience 2022Quote: ... 0.8 ul of each normalized sample was mixed with 2.4 ul of tagmentation mix containing Tn5 Tagmentation enzyme (20034198, Illumina) and then incubated at 55°C for 12 minutes ...
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bioRxiv - Neuroscience 2022Quote: ... and these reads were counted by htseq-count v0.5.3 (with intersection-strict mode and stranded option for RiboZero samples) according to gene annotation (Illumina iGenome), and RPKM was calculated ...
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bioRxiv - Microbiology 2023Quote: ... Approximately 120 million 125-bp paired-end reads per sample were obtained (HiSeq 2500, Illumina, San Diego, CA, USA). RNA-seq was performed by the Genomic core ...
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bioRxiv - Neuroscience 2023Quote: ... The sample concentration was adjusted to 2.8 nM before sequencing (50 bp single end) on a HiSeq 4000 (Illumina) using HiSeq 3000/4000 SR Cluster Kit and HiSeq 3000/4000 SBS Kit (50 cycles ...
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bioRxiv - Microbiology 2024Quote: ... Sequencing was performed for 32 total samples in MiSeq v2 250 bp paired-end format (Illumina, San Diego, CA).
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bioRxiv - Immunology 2024Quote: ... Samples were processed via the Chromium Next Gem Single Cell 3’ HT Dual Index v3.1 protocol and sequenced to a depth of 550 million read pairs per sample (∼23,000 read pairs per nucleus) on a NovaSeq 6000 system (Illumina).
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bioRxiv - Microbiology 2024Quote: ... Samples were sent for paired-end sequencing (2×250bp) on the Illumina MiSeq platform (Illumina, San Diego, CA, USA) at the Cornell University Biotechnology Resource Center (Ithaca ...
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bioRxiv - Microbiology 2022Quote: DNA libraries were generated for a total of 112 samples with Nextera DNA Flex (Illumina, Inc.; San Diego, CA). Resulting libraries were then visualized on a Tapestation 4200 (Agilent ...
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bioRxiv - Microbiology 2022Quote: ... Samples were paired-end sequenced on a single run of a MiSeq platform (Illumina, Inc., San Diego, CA, USA) at a length of 301 nucleotides (nt) ...
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bioRxiv - Genomics 2023Quote: ... about 40 ng purified pre-amplified Hi-C sample was fragmented in two 50 μl tagmentation mix (1x TD buffer and 0.5 μl TDE1 (Illumina Tagment DNA TDE1 Enzyme and Buffer Kit ...
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bioRxiv - Microbiology 2023Quote: ... and the samples were subjected to Illumina-based whole-genome sequencing using a MiSeq 250 paired-end run (Illumina). CLC Genomics Workbench (Qiagen ...
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bioRxiv - Physiology 2023Quote: ... with a sequencing depth of 25 M reads per sample on a NovaSeq platform (Illumina, San Diego, CA, USA).
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bioRxiv - Cancer Biology 2023Quote: ... All libraries were sequenced with a depth of at least 50,000 reads per spot (minimum of ~250 millions per sample) at the NovaSeq (Illumina).
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bioRxiv - Biophysics 2023Quote: ... Raw data was de-multiplexed and FASTQ files for each sample were generated using the bcl2fastq2 software (Illumina inc.).
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bioRxiv - Genomics 2023Quote: ... The H3K27ac ChIPseq bank construction was also done by Montpellier Genomix platform with TruSeq® ChIP Sample Preparation (Illumina) (GSE199512).
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Human CCR6+ Th cells show both an extended stable gradient of Th17 activity and imprinted plasticitybioRxiv - Immunology 2023Quote: ... pre-amplified samples were used for TaqMan quantitative PCR which was performed on Eco Real-Time PCR System (Illumina) using gene specific primers purchased from Fluidigm (DELTAgene Assay ...
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bioRxiv - Systems Biology 2023Quote: ... Samples were pooled for cBot amplification and sequenced as 75 bp paired-end reads on a NextSeq 500 (Illumina). Samples were demultiplexed with Bcl2fastq2 before analysis.
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bioRxiv - Immunology 2023Quote: ... cDNA amplification and library preparation (10X v3.1 dual index chemistry) were performed for samples according to manufacturer protocol and sequenced on a NovaSeq S4 (Illumina) to a depth of >30,000 reads/cell ...
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bioRxiv - Immunology 2023Quote: ... cDNA amplification and library preparation (10X v3.1 dual index chemistry) were performed for samples according to manufacturer protocol and sequenced on a NovaSeq S4 (Illumina) to a depth of >30,000 reads/cell ...
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bioRxiv - Cancer Biology 2023Quote: ... All samples were pooled equimolarly and sequenced on a NextSeq 500 High Output v2.5 flowcell (Illumina p/n 20024906) using the Illumina NextSeq 500 sequencing instrument with a single-read configuration (75 bp) ...
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bioRxiv - Molecular Biology 2023Quote: ... 15000 cells/sample for mESC were treated with Tagment DNA Buffer 2x reaction buffer with Tagment DNA Enzyme (Illumina) according to the manufacturer’s protocol ...
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bioRxiv - Cancer Biology 2023Quote: ... gDNA of 200,000 MNCs per sample was extracted and submitted to the DKFZ GPCF (Heidelberg, Germany) for Infinium MethylationEPIC BeadChip (Illumina) analysis ...
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bioRxiv - Neuroscience 2023Quote: ... Raw base calls were demultiplexed and converted into sample specific fastq files using default parameters of the bcl2fastq program (v 2.20, Illumina). Trimmed reads (TrimGalore ...
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bioRxiv - Molecular Biology 2023Quote: ... Fragmented genomic DNA libraries were produced from 10 ng of each sample treated with 1.5 µl of Nextera XT tagmentase (Illumina) at 37°C for 45 min with gentle shaking ...
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bioRxiv - Microbiology 2023Quote: ... The sample was sequenced across two lanes of a NovaSeq 6000 SP 2 × 150bp flowcell (Illumina, San Diego, CA) at the Ramaciotti Centre for Genomics (UNSW Sydney ...
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bioRxiv - Cell Biology 2023Quote: ... Paired end 38 bp sequences were generated from samples on a NextSeq 500/550 (Illumina, San Diego, CA, USA) with an average of 125 million of reads per sample.
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bioRxiv - Biochemistry 2023Quote: ... 30-50 million 100 bp paired-end reads were collected per sample using a NovaSeq 6000 Sequencing System (Illumina).