Labshake search
Citations for Illumina :
4001 - 4050 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.
-
bioRxiv - Cancer Biology 2022Quote: ... Paired-end libraries with 2 × 75 bp reads were prepared from the extracted RNA using the TruSeq Stranded total RNA LT Sample Prep (RiboZero Gold, Illumina) using Illumina methodology ...
-
bioRxiv - Evolutionary Biology 2022Quote: ... all the replicates were pooled by sample before purification and to proceed to the further preparation of the library according to the protocol outlined by Illumina (« 16S metagenomic Sequencing Library Preparation ») ...
-
bioRxiv - Microbiology 2022Quote: ... Dual-index paired-end sequencing of the throat samples was performed on the V4 region of the 16S rRNA gene on a MiSeq Desktop sequencer (M00984, Illumina), as previously described (De Boeck et al ...
-
bioRxiv - Microbiology 2022Quote: ... The generated data were subsequently demultiplexed using sample- specific barcodes and changed into fastq files using bcl2fastq (Illumina; version 1.8.4). The quality of the data was assessed using FastQC (v0.11.8 ...
-
bioRxiv - Developmental Biology 2022Quote: ... The library samples were then diluted to the final concentration of 10nM and loaded onto two lanes of the NovaSeq 6000 (Illumina) instrument flow-cell for a 100-cycle sequencing run ...
-
bioRxiv - Cancer Biology 2022Quote: ... Libraries were generated from 1 μg of total RNA using a TruSeq Stranded Total RNA Library Prep Human/Mouse/Rat (48 Samples) (Illumina) per manufacturer’s instructions ...
-
bioRxiv - Developmental Biology 2021Quote: ... Sequencing of 12 liver samples (with 84 unrelated samples) was performed using a single NovaSeq S1 200 cycle sequencing run on a NovaSeq 6000 machine (Illumina) through IMB Sequencing Facility ...
-
bioRxiv - Molecular Biology 2020Quote: ... RNA samples with RIN>8.0 were shipped to Beijin Genome Institute for a library preparation and sequencing (Illumina HiSeq 2500). Integrative Genomics Viewer (2.4.14 Broad Institute ...
-
bioRxiv - Molecular Biology 2020Quote: ... The resulting libraries were minimally amplified to enrich for fragments using adapters on both ends and then quantified for sequencing at eight samples/flow cell by using a NextSeq 500/550 (Illumina) sequencer (PE 150).
-
bioRxiv - Microbiology 2021Quote: ... All RNA-seq and RIP-seq experiments were performed thrice with RNA samples obtained from independently prepared mycelia using the NextSeq 500 system (Illumina) and mapped to the A ...
-
bioRxiv - Immunology 2021Quote: ... Libraries were sequenced by paired end (2x75 bp) to a depth of 25 million reads per sample (Illumina Miseq v3).
-
bioRxiv - Cancer Biology 2020Quote: Genomic DNA from 28 samples in which scDNA-seq data showed at least 5% of homozygously mutated clones were analyzed by Illumina Omni2.5-8 SNP array ...
-
bioRxiv - Neuroscience 2022Quote: ... We pooled libraries from different samples based on molar concentrations and sequenced them on a NextSeq 500 or NovaSeq 6000 instrument (Illumina) with 28 bases for read 1 (26 bases for v2 libraries) ...
-
bioRxiv - Genomics 2022Quote: ... refringens positive and negative samples were generated for RNAseq library construction and sequencing using the same protocol as described above and sequenced by Illumina HiSeq 2×150 cycles run (Illumina Inc. ...
-
bioRxiv - Cancer Biology 2022Quote: ... The bead-bound fragments are then amplified and sample indexed using P5 and RPI-X (binds the TruSeq Small RNA Read 2 handle and adds a sample index and P7 Illumina sequencing handle ...
-
bioRxiv - Cell Biology 2019Quote: ... The purified RNA samples were processed for preparations of cDNA libraries using the TruSeq Stranded Total RNA Ribo-Zero H/M/R (Illumina) and sequenced on HiSeq-2500 platform (Illumina ...
-
bioRxiv - Molecular Biology 2019Quote: The clustering of the index-coded samples was conducted on an acBot Cluster Generation System using TruSeq PE Cluster Kitv3-cBot-HS (Illumina) following the manufacturer’s instructions ...
-
bioRxiv - Microbiology 2019Quote: ... “preterm” OR “newborn” to find all available publications where newborn gut samples (with sampling on days 0 to 36 of life) had been shotgun metagenome sequenced using NextSeq of HiSeq (Illumina) with read lengths from 100 to 250 basepairs ...
-
bioRxiv - Microbiology 2019Quote: ... Libraries for all samples were sequenced as 150 bp paired-end reads on a single lane of Illumina Hi-Seq 4000 (Illumina). Reads were bioinformatically de-multiplexed ...
-
bioRxiv - Genomics 2019Quote: The assembly used heterozygous parameters due to the relatively high heterozygosity of the sample (2.13% estimated from Genoscope 93 and previous Illumina sequencing). BUSCO v3 40 was run using the metazoa_odb9 gene set with the command:
-
bioRxiv - Genomics 2020Quote: ... was used to construct poly(A) selected paired-end sequencing libraries according to TrueSeq Stranded mRNA Sample Preparation Guide (Illumina). All libraries were quantified with the Fragment Analyzer (Advanced Analytical Technologies) ...
-
bioRxiv - Bioengineering 2019Quote: ... cDNA was amplified by 15 PCR cycles and 10-11 samples were pooled before sequencing for 100 base pair single-end reads on a HiSeq 4000 instrument (Illumina).
-
bioRxiv - Genomics 2019Quote: ... For HapMap samples and three PGT-M families paired-end (2×125bp) sequencing was performed on a HiSeq2500 system (Illumina) in multiple runs ...
-
bioRxiv - Zoology 2019Quote: ... Genomic DNA of these six samples were sent from Andalas University for Illumina HiSeq 4000 (Illumina Inc., San Diego, CA) sequencing (150 PE ...
-
bioRxiv - Developmental Biology 2020Quote: ... 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 (26 bases for v2 libraries) ...
-
bioRxiv - Cancer Biology 2020Quote: ... 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 mouse reference genome (GRCm38/mm10 ...
-
bioRxiv - Molecular Biology 2020Quote: ... An additional QC measure to determine the concordance of average beta values generated for seven duplicate samples was completed using GenomeStudio (Illumina) v1.8 ...
-
bioRxiv - Cancer Biology 2021Quote: ... RNA was purified from total RNA samples (100-500 ng) with oligo(dT) magnetic beads and sequencing libraries recommended by Illumina. Purified libraries were qualified on an Agilent Technologies 2200 TapeStation using a D1000 ScreenTape assay (cat# 5067-5582 and 5067-5583) ...
-
bioRxiv - Pharmacology and Toxicology 2021Quote: ... The generated data were subsequently demultiplexed using sample-specific barcodes and changed into fastq files using bcl2fastq (Illumina; version 1.8.4). The quality of the data was assessed using FastQC (75) ...
-
bioRxiv - Molecular Biology 2021Quote: ... Samples with RNA integrity number (RIN) > 9 were used for sequencing library construction with the TruSeq Stranded mRNA sample preparation protocol (Illumina).
-
bioRxiv - Plant Biology 2020Quote: ... A total of 56 samples (Appendix 1) were sequenced together on one lane of 1×75bp NextSeq500 High Output (Illumina).
-
bioRxiv - Genomics 2020Quote: ... prepared samples were pooled into two pools (with 10 and 14 individuals each) for sequencing on a HiSeq 4000 (Illumina) using paired-end (PE ...
-
bioRxiv - Neuroscience 2020Quote: ... following manufacturer instruction followed by paired-end sequencing at 100M read depth for each sample (Illumina, Otogenetics, Atlanta - GA, US). Raw .fastq sequences were cleaned from any residual sequencing adapter using cutadapt with parameters -m 20 and -e 0.1 ...
-
bioRxiv - Neuroscience 2019Quote: ... Linear amplified aRNA from cell bodies and axon samples (2 biological replicates each) was used to prepare RNASeq libraries using the strand-specific ScriptSeq protocol (Illumina). Paired-end sequencing (2x 150bp ...
-
bioRxiv - Cancer Biology 2021Quote: cDNA from tonsil and breast cancer tissue microregion samples were prepared into sequencing libraries using Nextera XT library preparation (Illumina), while cDNA from melanoma microregion libraries were prepared with ThruPLEX DNA-seq Kit (Takara Bio) ...
-
bioRxiv - Immunology 2020Quote: ... RNA libraries were then prepared from two biological replicates per condition and samples were sequenced using 75 base pair single-end reading on HiSeq 2500 high-output instrument (Illumina). The raw reads were then subjected to trimming by Trim Galore (https://github.com/FelixKrueger/TrimGalore ...
-
bioRxiv - Genomics 2021Quote: ... Samples underwent library preparation and 50 bp single end (SE) NGS sequencing using an Illumina HiSeq2000 (Illumina, San Diego CA) at the USC Epigenome Center (USC ...
-
bioRxiv - Molecular Biology 2021Quote: ... Genomic DNA samples were processed further at the Barts and the London Genome Centre and run on Infinium MethylationEPIC arrays (Illumina).
-
bioRxiv - Biochemistry 2021Quote: ... The quality of libraries was assesses based on size distribution and concentration using 2100 Bioanalyzer with DNA 1000 chip (Agilent Technologies. All samples were sequenced 25M reads on an Illumina NovaSeq 6000 Sequencer using the 2×50bp paired-end platform.
-
bioRxiv - Cancer Biology 2021Quote: ... Barcoded libraries of ten samples (4 treated, 4 untreated and two controls) were equimolarly pooled and sequenced on MiSeq (Illumina) using MiSeq v3 150 reagent kit (MS-102-3001 ...
-
bioRxiv - Genomics 2020Quote: ... Replicas of each 384 sample pools were loaded onto the S4-flow cell following NovaSeq-XP workflow as per the manufacturer’s instructions (Illumina Inc). Dual indexed single end sequencing with 36bp read length was carried out on NovaSeq 6000 platform.
-
bioRxiv - Cancer Biology 2021Quote: ... 9 samples with DNA >40kbp were concurrently sequenced using PacBio and Illumina and the remaining 13 tumor samples were sequenced by Illumina WGS only ...
-
bioRxiv - Cancer Biology 2021Quote: ... sequencing of samples for which RNA of sufficient quality and quantity was available was performed on a NextSeq 500 instrument (Illumina) as previously described 17 ...
-
bioRxiv - Microbiology 2021Quote: ... Samples were sequenced using an Illumina MiSeq for 250 X 250 bp paired-end sequencing (Illumina, San Diego, CA, USA). Samples were demultiplexed by the facility ...
-
bioRxiv - Evolutionary Biology 2020Quote: ... Sequencing libraries were prepared by LC Sciences following Illumina’s TruSeq-stranded-total-RNA-sample preparation protocol (Illumina, San Diego, USA). Quality control analysis and quantification of the sequencing library were performed using Agilent Technologies 2100 Bioanalyzer High Sensitivity DNA Chip ...
-
Comparative effectiveness of probiotic-based formulations on cecal microbiota modulation in broilersbioRxiv - Microbiology 2019Quote: ... DNA samples were library prepared for NGS using the Illumina MiSeq platform (2 × 300 bp; Illumina, San Diego, CA, USA) by Ohio State University Molecular and Cellular Imaging Center.
-
bioRxiv - Immunology 2020Quote: ... Indexed samples were pooled together for 100 cycles of paired end sequencing on a HiSeq 4000 or HiSeq 2500 system (Illumina). More than 40 million reads per sample were sequenced for downstream analysis.
-
bioRxiv - Developmental Biology 2021Quote: ... libraries were also prepared using 50 ng of gDNA isolated from NaR P5 and 3D-RA DD25 cells by following the Nextera DNA Sample Preparation Guide (Illumina). The libraries were purified using the MinElute PCR purification kit (Qiagen ...
-
bioRxiv - Cell Biology 2021Quote: ... pooled and sequenced 75 bp paired-ended (human samples) or single-end (cultured and sorted fibroblasts) on the NextSeq 500 (Illumina).
-
bioRxiv - Genetics 2020Quote: ... Samples were multiplexed and paired-end sequencing was performed using either a MiniSeq or NovaSeq 6000 (Illumina; San Diego, CA).