Labshake search
Citations for Illumina :
4051 - 4100 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 - Cancer Biology 2020Quote: ... were used to optimize the cDNA amplicon size followed by adding P5 and P7 sample indexes (used in Illumina sequencers), and Illumina R2 sequence via processes of end repair ...
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bioRxiv - Cancer Biology 2022Quote: ... whole-genome and targeted libraries were added to flow cell in a 67%-33% ratio and sequenced to approximately 16M fragments per sample corresponding to ~1-2x whole genome coverage using NovaSeq S4 sequencing (Illumina) with 150 bp paired-end reads.
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bioRxiv - Molecular Biology 2022Quote: ... libraries were submitted to the Genomics and Microarray Shared Resource at the University of Colorado Anschutz Medical Campus for sequencing of 10 million paired end reads per sample on the NovaSEQ6000 (Illumina).
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bioRxiv - Cell Biology 2022Quote: ... Samples were randomised to avoid batch effects and multiplexed libraries were run on a single lane (8 samples/lane) of the HiSeq 4000 platform (Illumina) to generate 50bp single-end reads ...
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bioRxiv - Cell Biology 2022Quote: ... Samples were randomised to avoid batch effects and multiplexed libraries were run on a single lane (8 samples/lane) of the HiSeq 2500 platform (Illumina) to generate 100bp paired-end reads ...
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bioRxiv - Developmental Biology 2022Quote: ... Between 59M and 130M reads were sequenced per sample in a 100bp paired-end format using a NovaSeq 6000 (Illumina) platform ...
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bioRxiv - Genomics 2022Quote: ... Samples were sequenced with a coverage of 50 M paired end reads (2 x 100 bp) /sample on a NovaSeq (Illumina).
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bioRxiv - Synthetic Biology 2022Quote: Sample concentrations were measured with the Qubit and 38 µL of each sample was submitted to the Tufts Genomics Core for TruSeq ChIP library preparation (Illumina). Tufts Genomics Core subsequently sequenced all samples ...
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bioRxiv - Microbiology 2022Quote: ... We performed 150 bp paired-end RNA sequencing on all samples that yielded RNA using a NovaSeq 6000 (Illumina, Inc.).
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bioRxiv - Genomics 2022Quote: ... Clustering of the index-coded samples was performed on an acBot Cluster Generation System using TruSeq PE Cluster Kitv3-cBot-HS (Illumina) according to the manufacturer’s instructions ...
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bioRxiv - Microbiology 2023Quote: ... Sequencing was performed at 5 million reads/sample in single-end mode with 150 nt read length on the NextSeq 500 platform (Illumina) using a Mid output sequencing kit ...
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bioRxiv - Cancer Biology 2024Quote: ... Equimolar libraries from each sample were pooled and subjected to 75-bp paired-end sequencing on a NextSeq 550 machine (Illumina). Raw reads were demultiplexed and FASTQ files were generated using Bcl2fastq v2.20.0.422 (Illumina) ...
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bioRxiv - Cancer Biology 2024Quote: ... the sequencing was performed under the setting of single read 1×51 bp to generate ∼30 million reads per sample on HiSeq 1000 sequencer (Illumina).
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bioRxiv - Physiology 2022Quote: ... was performed at 25 million reads/sample in single-end mode with 75 nt read length on the NextSeq 500 platform (Illumina) using High output sequencing kit ...
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bioRxiv - Neuroscience 2022Quote: ... Libraries were pooled from different samples based on molar concentrations and sequenced with 1% PhiX spike-in on a NextSeq 500 instrument (Illumina) with 33 bases each for read 1 and read 2 ...
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bioRxiv - Neuroscience 2022Quote: ... We pooled libraries from different samples based on molar concentrations and sequenced them on a NextSeq 500 or NovaSeq instrument (Illumina) with 28 bases for read 1 ...
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bioRxiv - Molecular Biology 2024Quote: ... CUT&RUN libraries (10–20 Mio reads per sample and 1/3 of reads for the controls) were sequenced on a NovaSeq 6000 (Illumina) paired end 100 bp at the Deep Sequencing Facility (Max Planck Institute for Immunobiology and Epigenetics ...
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bioRxiv - Bioengineering 2024Quote: ... The PCR amplicons were cleaned up and unique indexes attached to the samples before being run on a MiSeq v2 chip (Illumina), read depth >10000 per sample ...
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bioRxiv - Cell Biology 2023Quote: ... DNA samples were quality checked and subjected to library preparation in alignment with the 16S metagenomic library preparation protocol from Illumina Inc ...
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bioRxiv - Cell Biology 2024Quote: ... Strand-specific 354 mRNA sequencing was performed on total RNA and using TruSeq stranded mRNA sample prep 355kit LT (Illumina) (Roques et al. ...
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bioRxiv - Genetics 2024Quote: ... we aligned the corresponding short reads to the human reference GRCh38 using bwa mem23 (v 0.7.17-r1188; -t 48 -R “@RG\tID:1\tLB:lib1\tPL:ILLUMINA\tSM:<sample name>\tPU:unit1”). Next ...
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bioRxiv - Neuroscience 2024Quote: ... RNA was analyzed using a BioAnalyzer and samples with 8.7-10.0 RNA integrity number values were used for library preparation using the Illumina TruSeq RNA Sample Preparation v2 Guide (Illumina). Libraries were sequenced on an Illumina NextSeq 500 as 42bp paired-end reads (PE42) ...
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bioRxiv - Developmental Biology 2024Quote: ... 250,000 cells per sample were submitted to the VBC NGS facility for further processing and ATAC-seq library preparation (Bulk ATAC-seq Illumina). In brief ...
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bioRxiv - Genomics 2024Quote: ... leaf and flower samples from three biological replicates of Huizhan and ZH11 were collected and sequenced on the NovaSeq 6000 platform (Illumina) following the manufacturers’ recommended procedures.
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bioRxiv - Developmental Biology 2024Quote: ... Amplification was carried out using 3 µl of NMP per sample and adding 1 µl of each dual-indexed (i7 and i5; Illumina) primer ...
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bioRxiv - Developmental Biology 2024Quote: ... Another cleanup step with SPRIselect was performed before the Sample Index PCR when P5 and P7 sequences (for Illumina sequencing) and sample indices (to allow for multiplexing in the sequencer ...
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bioRxiv - Immunology 2024Quote: ... PCR was performed using 4 µL of each sample and the oligos from each ROI were indexed using unique i5 and i7 dual-indexing systems (Illumina). PCR reactions were purified twice using AMPure XP beads (Beckman Coulter ...
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bioRxiv - Genetics 2023Quote: Sequence libraries were pooled into groups of 16 samples and sequenced on the Illumina MiSeq System (Illumina, San Diego, CA) with the MiSeq Reagent Kit v2 (300 cycles ...
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bioRxiv - Immunology 2024Quote: ... The molar concentration of the amplicon from each sample was normalized and then sequenced on a NextSeq 500/550 instrument (Illumina). The purified Kinome CRISPR Knockout Library plasmids were also PCR-amplified and sequenced using the same procedure to verify the integrity of the sgRNA library.
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bioRxiv - Genetics 2023Quote: ... 30 million paired-end 150bp reads were obtained for each ChIP-ISO and input sample using a NextSeq 2000 (Illumina) instrument ...
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bioRxiv - Genomics 2023Quote: ... ChIP DNA was then prepared for Illumina multiplex-sequencing with 10 samples per lane at 65 bp single end and sequenced on Illumina HiSeq 2500 (Illumina).
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bioRxiv - Developmental Biology 2023Quote: ... to an average read depth of 40 million reads per sample using the Illumina HiSeq platform (Illumina, San Diego, CA). The raw RNA sequencing data was examined using FastQC (https://www.bioinformatics.babraham.ac.uk/projects/fastqc/) ...
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bioRxiv - Genomics 2022Quote: All samples (n=75) underwent 16S rRNA gene sequencing using 515F-806R primers on the MiSeq (Illumina, San Diego, USA) as previously described (Seaton et al. ...
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IRF1 regulates self-renewal and stress-responsiveness to support hematopoietic stem cell maintenancebioRxiv - Cell Biology 2023Quote: ... Sequencing was performed using Nova Seq S4 (run type: PE100, type of library: NexteraXT, 25 million reads per sample; Illumina). Preprocessing and analysis were done using Galaxy Quality and adapter trimming of reads was performed using RNA Galaxy workbench 2.058 ...
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bioRxiv - Microbiology 2023Quote: ... We stored the DNA at −80° C and an aliquot from each sample was used for sequencing using a MiSeq sequencer (2 × 250 bp, Illumina). A first run was sent to the Integrated Microbiome Resource (Halifax ...
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bioRxiv - Microbiology 2023Quote: ... Samples were DNAse-treated and sent for library preparation and mRNA-seq by NUcore (Northwestern) on a HiSeq 4000 (Illumina) with 50 bp single-end reads ...
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bioRxiv - Genomics 2023Quote: ... all samples were pooled at 4 nm concentration and paired-end [300bp (2 × 151bp)] sequenced in MiSeq platform (Illumina, USA).
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bioRxiv - Neuroscience 2023Quote: ... performed paired-end next-generation RNA sequencing with a depth of 60 million reads per sample on the NovaSeq platform (Illumina) at the University of Michigan Advanced Genomics Core ...
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bioRxiv - Plant Biology 2023Quote: ... and paired-end transcriptome sequencing of each sample was conducted using an Illumina NovaSeq6000 sequencer (Illumina, San Diego, CA, USA). Over a total of 30 million 101 base paired-end reads were obtained (Suppl ...
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bioRxiv - Microbiology 2023Quote: ... DNA-Seq libraries were prepared using Nextera XT library preparation kit with 700 pg DNA input per sample and 6:30 min tagmentation at 55 °C and barcoded using Nextera XT indexes (Illumina). RNA-Seq libraries were prepared using KAPA RNA HyperPrep kit (Roche ...
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bioRxiv - Genomics 2023Quote: ... The PhiX Control library was spiked in the sequencing sample at 10% (v/v) (Illumina, cat. no. FC-110-3001).
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bioRxiv - Molecular Biology 2023Quote: ... Libraries with unique dual indexes were pooled and sequenced on partial lanes targeting ∼50M reads per sample on a HiSeq or a NovaSeq 6000 sequencer (Illumina) using 150-bp paired-end sequencing chemistry.
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bioRxiv - Microbiology 2023Quote: ... was performed at 10 million reads/sample in single-end mode with 75 nt read length on the NextSeq 500 platform (Illumina) using High output sequencing kits ...
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bioRxiv - Cell Biology 2023Quote: ... The generated data were subsequently demultiplexed using sample-specific barcodes and changed into fastq files using bcl2fastq (Illumina; version 1.8.4). Reads were afterwards aligned to the human reference genome (GRCh38/hg38 ...
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bioRxiv - Genomics 2023Quote: ... The pooled libraries were sequenced in the 2 × 150bp format to an average depth of 300 million reads/sample on a NovaSeq 6000 S4 (Illumina) by Psomagen Inc.
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bioRxiv - Microbiology 2023Quote: ... All eighteen samples were sequenced as a multiplexed library on a single lane of a HiSeq 4000 sequencing system (Illumina), generating 200 nt paired end reads.
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bioRxiv - Genomics 2023Quote: ... Single-end reads of 75 basepairs were generated for each sample on an Illumina NextSeq 500 (Illumina, San Diego, CA). Raw data files were uploaded to Gene Expression Omnibus with accession number GSE216035.
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bioRxiv - Microbiology 2023Quote: ... under each condition (30Mb read/each sample) was loaded on the Illumina Nextseq 500 system with a NextSeq 500/550 High Output Reagent CartriDEG v2 (Illumina) for single-end reads at Carnegie Embryology Department’s in-house sequencing facility ...
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bioRxiv - Immunology 2023Quote: ... was performed at 19-36 million reads/sample in single-end mode with 75 nt read length on the NextSeq 500 platform (Illumina) with 1 High Output Kit v2.5 ...
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bioRxiv - Neuroscience 2023Quote: ... DNA samples for available twin participants were genotyped using the Infinium Global Screening Array-24 v3.0 BeadChip (Illumina, California, USA). Genotyping data is expected to be available in 2023 ...