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Citations for Illumina :
401 - 450 of 686 citations for Family With Sequence Similarity 46 Member B FAM46B Antibody since 2019
Citations are collected from bioRxiv only, the total number of publications could be much larger.
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bioRxiv - Genetics 2020Quote: Raw sequence data was converted to FASTQ format using the bcl2fastq conversion software v2.17.1.14 (Illumina, Inc) and analysed using the pipeline described in Beal et al. ...
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bioRxiv - Genomics 2021Quote: ... Paired-end sequence reads (PE150) were generated using an Illumina NovaSeq 6000 platform (Illumina Inc., USA).
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bioRxiv - Microbiology 2020Quote: Sequence libraries for Illumina sequencing were prepared using the Nextera XT kit (Illumina, San Diego, CA) according to the manufacturer’s instructions with 1 ng genomic DNA as input ...
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bioRxiv - Immunology 2022Quote: ... Sequence libraries were constructed and then quantified by qpcr using the KAPA Library Quant Kit (Illumina) from KAPA Biosystems (Roche ...
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bioRxiv - Microbiology 2023Quote: ... The sequence library was prepared using SMARTer Stranded RNA-Seq Kit (Illumina, San Diego, CA, USA), and next-generation sequencing analysis was conducted using NovaSeq 6000 (100-bp paired-end reads ...
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bioRxiv - Microbiology 2022Quote: ... was used to sequence the library with a 2×300 bp cycle with 15% PhiX (Illumina). All raw sequence data have been deposited in the NCBI SRA (accession number pending).
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bioRxiv - Cancer Biology 2023Quote: ... appropriate sequence primer sites and adapters were added for sequencing on a NextSeq 500 sequencer (Illumina). After sequencing ...
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bioRxiv - Microbiology 2023Quote: ... genomic DNA from parental and mutant cell lines were sequenced by the HiSeq4000 sequence system (Illumina), generating about 10 million 100-bp reads and compared to that of the T ...
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bioRxiv - Genomics 2023Quote: The genome sequence of Wolbachia wOcae from the mason bee Osmia caerulescens was assembled from Illumina reads available under NCBI SRA accession SRR1221705 ...
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bioRxiv - Plant Biology 2023Quote: ... 150 bp paired-end sequences were generated using an Illumina NovaSeq 6000 (Illumina, San Diego, California).
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bioRxiv - Microbiology 2023Quote: ... 51-bp Single Read sequences were generated on the Hiseq2000 sequencer according to manufacturer’s instructions (Illumina). Reads were processed ...
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bioRxiv - Microbiology 2023Quote: Raw sequence data were demultiplexed into sample-specific fastq files using bcl2fastq conversion software from Illumina. Adapter residues were trimmed from both the 5′- and the 3′-end of the reads using the AdapterRemoval v292 ...
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bioRxiv - Microbiology 2023Quote: ... 150 bp paired-end stranded sequences were generated on a NovaSeq S4 (Illumina, San Diego, USA). The experiment was performed with three biological replicates ...
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bioRxiv - Cancer Biology 2024Quote: ... a sequence library was prepared using the TruSeq Nano DNA Kit (Illumina, San Diego, CA, USA), and next-generation sequencing analysis was conducted using a NovaSeq 6000 (150-bp pair-end reads ...
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bioRxiv - Developmental Biology 2020Quote: ... with TruSeq RNA Single Indexes Set A and B (Illumina, Cat. No. 20020492 and 20020493). Resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent ...
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bioRxiv - Synthetic Biology 2021Quote: ... 16S rRNA genes were amplified using the primers described below (Illumina Part #15044223 Rev. B) and sequenced using Sanger sequencing (Eton Biosciences ...
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bioRxiv - Evolutionary Biology 2023Quote: ... and TruSeq RNA Single Indexes Sets A and B (Illumina Cat. No. 20020492 and 20020493). Resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent ...
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bioRxiv - Developmental Biology 2021Quote: ... and were sequenced on the Illumina NovaSeq (>70 million 2×150 bp sequences) (Illumina, San Diego, CA).
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bioRxiv - Evolutionary Biology 2020Quote: ... The MEGA-Ex array probe sequences used to genotyped the BioVU cohort were obtained directly from Illumina. Probes sequence for the UK Axiom Biobank array (Resource 149601 ...
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bioRxiv - Genomics 2022Quote: ... Reads were trimmed using the FASTX-Toolkit (Version 0.013 - http://hannonlab.cshl.edu/fastx_toolkit/) to remove linker sequences (Illumina adaptors) and then filtered for a minimum sequencing quality of 30 in 50% of the bases ...
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Data-driven modelling of mutational hotspots and in-silico predictors in hypertrophic cardiomyopathybioRxiv - Genetics 2020Quote: ... High-coverage exonic sequences were captured by target enrichment and sequenced on the MiSeq platform (Illumina Inc.). Joint bioinformatic processing of both datasets followed the Genome Analysis ToolKit version 4 best practice guidelines (S1B Methods) ...
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bioRxiv - Neuroscience 2020Quote: ... The resulting base call files (.bcl) were converted to standard fastq formatted sequence files using Bcl2Fastq (Illumina). Sequencing quality was assessed using FastQC (Babraham Bioinformatics ...
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bioRxiv - Neuroscience 2020Quote: ... The resulting base call files (.bcl) were converted to standard fastq formatted sequence files using Bcl2Fastq (Illumina). Sequencing quality was assessed using FastQC (Babraham Bioinformatics ...
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bioRxiv - Molecular Biology 2020Quote: ... libraries were quantified by Qubit and sent to sequence SR75 bp on a HiSeq 4000 platform (Illumina). Results coming from the deep sequencing have been analyzed as follow ...
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bioRxiv - Cell Biology 2021Quote: Sequence analysis was performed by mapping the paired-end 42 bp sequencing reads (PE42) generated by Illumina sequencing (using NextSeq 500 ...
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bioRxiv - Cancer Biology 2020Quote: ... sequence data were demultiplexed and Fastq files were generated using Bcl2Fastq2 conversion software provided by Illumina (v2.20.0.422).
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bioRxiv - Microbiology 2020Quote: Illumina sequence libraries of genomic DNA were prepared using the Nextera XT kit (Illumina, San Diego, CA) according to the manufacturer’s instructions ...
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bioRxiv - Genomics 2022Quote: ... ciliaris (deposited in SRA Sequence Read Archive under accession SRR8666664, Illumina HiSeq 2500; Nevill et al., 2020) were downloaded and used to discover the most abundant repetitive DNA sequences ...
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bioRxiv - Microbiology 2019Quote: ... for 2 hours at 25 °C and reverse transcription was performed with Reverse Transcription Primer (Illumina sequence) using SuperScript IV Reverse Transcriptase (ThermoFisher ...
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bioRxiv - Molecular Biology 2020Quote: ... The libraries were pooled and 50-bp single-end sequences were obtained using the HiSeq4000 sequencer (Illumina) in Vincent J ...
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bioRxiv - Developmental Biology 2019Quote: ... Sequence data were demultiplexed and Fastq files were generated using Bcl2Fastq conversion software (Illumina, San Diego, CA).
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bioRxiv - Genomics 2021Quote: ... Nucleotide sequences of the libraries were determined with theHiSeq 2500 DNA sequencing system (Illumina, San Diego, CA) in paired-end ...
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bioRxiv - Plant Biology 2021Quote: ... Seventy-five bp single-read sequences were generated using the NextSeq500 (Illumina, Inc., San Diego, C, USA) instrument ...
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bioRxiv - Molecular Biology 2021Quote: ... sequencing and analysis of sequence data were performed in accordance with the standard protocol described by Illumina and Novogene ...
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bioRxiv - Microbiology 2021Quote: ... Paired-end 150 bp sequences were generated using the Illumina HiSeq3000 System (Illumina, San Diego, CA, USA) with an average total yield of 2.5 Gbp per sample (2,548 ± 715 Mbp (mean ± SD)) ...
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bioRxiv - Immunology 2022Quote: ... The overall sequence depth was ~ 50000 reads/cell using the NovaSeq 6000 platform (Illumina, San Diego, CA). The demultiplexed reads obtained from NovaSeq were first aligned to a reference human genome assembly (GRCh38-3.0.0 ...
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bioRxiv - Microbiology 2023Quote: ... Sequencing was performed as a Single Read Multiplexed run for 65Lbp sequences on HiSeq 2500 sequencer (Illumina). The multiplexing level was 6 samples per lane ...
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bioRxiv - Microbiology 2023Quote: ... amplicon sequence libraries were prepared using the Nextera XT DNA library preparation kit (Illumina, San Diego, CA) according to the manufacturer’s protocol ...
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bioRxiv - Microbiology 2023Quote: The shotgun metagenome sequence library was prepared using the Nextera XT DNA library kit (Illumina, California, USA) as previously described [43] ...
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bioRxiv - Molecular Biology 2023Quote: ... A 206 bp library fragment was generated using overlap PCR and included NexteraXT adapter overhang sequences (Illumina 16S Metagenomic Sequencing Library Preparation protocol ...
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bioRxiv - Systems Biology 2023Quote: ... The raw Illumina amplicon sequence data was uploaded to BaseSapce Website (Illumina, San Diego, CA, United States) to assess sequence run quality and completion ...
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bioRxiv - Immunology 2024Quote: ... Sequence libraries were multiplexed and sequencing was performed using a 2x 150 paired end configuration (Illumina HiSeq). Raw data files were converted to fastq files ...
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bioRxiv - Microbiology 2024Quote: ... Sequence libraries were prepared using the Nextera XT DNA Library Preparation Kit (Illumina, San Diego, CA, USA) and Integrated DNA Technologies unique dual indexes (San Diego ...
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bioRxiv - Molecular Biology 2024Quote: ... 75-bp single read sequences were generated on the NextSeq 500 sequencer according to manufacturer’s instructions (Illumina).
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bioRxiv - Microbiology 2024Quote: ... Sequence libraries were generated using the TruSeq Stranded Total RNA Library Prep kit (Illumina, San Diego, CA) following the manufacturer’s recommendations ...
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bioRxiv - Plant Biology 2019Quote: ... Libraries were constructed using Illumina TruSeq RNA Single Indexes (Set A and B; Illumina, CA, USA) in a 14-cycle indexing PCR reaction ...
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bioRxiv - Microbiology 2020Quote: ... B) Informatics benchmarking (‘Experiment 2’) in which a seawater virome was sequenced with short-reads (Illumina) and long-read sequencing ...
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bioRxiv - Plant Biology 2020Quote: Illumina library preparation followed a modification of the Illumina 16S metagenomic protocol (Illumina #15044223 Rev. B) where all loci specific primers have a 33 bp tail added to the 5’ end ...
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bioRxiv - Genetics 2023Quote: ... B-allele frequency (BAF) and log-likelihood (LRR) data were generated using GenomeStudio v2.0.5 (Illumina Inc.) with a custom cluster file created according to the manufacturer’s instructions ...
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bioRxiv - Genetics 2021Quote: ... The detection of the nucleotide sequence was done on the Illumina NovaSeq6000 platform using the according kit (Illumina).