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Citations for Illumina :
201 - 250 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 - Microbiology 2022Quote: ... and sequences were generated on the Illumina MiSeq platform (Illumina). Raw reads were filtered using the Lotus pipeline (Hildebrand et al. ...
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bioRxiv - Plant Biology 2023Quote: ... and automatically de-multiplexed by the BaseSpace Sequence Hub (Illumina).
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bioRxiv - Genomics 2023Quote: Further validation of the mitogenome sequence was performed by Illumina reference short reads ...
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bioRxiv - Microbiology 2023Quote: ... Fastq sequence files were generated using bcl2fastq version 2.20 (Illumina). The samples went through two steps of quality assessment ...
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bioRxiv - Microbiology 2024Quote: ... Initial read processing involved contaminant scanning (e.g., Illumina adapter sequences) and quality-based cleaning using FastQC [49] ...
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bioRxiv - Cell Biology 2020Quote: ... Reference sequence assembly and transcript annotation that was obtained from Illumina iGenomes ...
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bioRxiv - Evolutionary Biology 2021Quote: ... The libraries were run on a sequence (Hiseq, Illumina, Tokyo, Japan). The library preparation and sequencing were performed by Genewiz Strand-Specific RNA-seq service ...
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bioRxiv - Neuroscience 2021Quote: ... Sequences were generated on a HiSeq2500 (Illumina, San Diego, CA, USA) as 125-bp paired-end runs ...
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bioRxiv - Cell Biology 2022Quote: ... Sequence data were extracted in FastQ format using bcl2fastq v1.8.4 (Illumina) and used for mapping approach ...
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bioRxiv - Genetics 2020Quote: ... raw sequencing reads were demultiplexed based on index sequences by Illumina’s BaseSpace ...
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bioRxiv - Genetics 2020Quote: ... and a selected RPIX index primer (Illumina sequences, ordered through IDT). Libraries were amplified for 8 PCR cycles ...
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bioRxiv - Genomics 2020Quote: ... the same reference DNA sequences (Illumina short read inserts 300 bp) were aligned to the chromosomes to detect homozygous deletions in the read alignments using Manta [82] ...
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bioRxiv - Cancer Biology 2021Quote: ... sample index and Illumina adapter sequences (Illumina Inc; San Diego, CA) were added ...
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bioRxiv - Plant Biology 2021Quote: ... paired-end sequences were obtained using the Hiseq X System (Illumina), after which assembly was performed using the HiRise software pipeline (Dovetail Genomics) ...
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bioRxiv - Microbiology 2021Quote: The genome sequences of representative edited clones were sequenced by Illumina technique ...
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bioRxiv - Pharmacology and Toxicology 2021Quote: ... The RNA sequence libraries were prepared using NeoPrep (Illumina, CA, USA) with Illumina TruSeq stranded mRNA Library kit for NeoPrep (Illumina ...
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bioRxiv - Genomics 2021Quote: ... Short-read sequence data were obtained using the HiSeq2000 platform (Illumina). Genome size was estimated using Jellyfish after removing adaptor sequences (AGATCGGAAGAGC ...
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bioRxiv - Microbiology 2022Quote: ... raw sequence files were demultiplexed using BaseSpace (Illumina, La Jolla, CA), and uploaded to Qiita [39] for additional pre-processing ...
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bioRxiv - Physiology 2020Quote: ... The demultiplexing of sequence data (from BCL files generated by Illumina sequencing systems to standard FASTQ file formats ...
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bioRxiv - Genetics 2020Quote: ... The formatted reference sequence file for BWA was provided by Illumina. The TASSEL4 GBS pipeline provided the HapMap file containing high-throughput SNPs (10,424 SNPs) ...
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bioRxiv - Evolutionary Biology 2021Quote: ... short-read sequence data (Illumina HiSeq 2×150bp paired-end reads) were ...
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bioRxiv - Evolutionary Biology 2021Quote: ... The libraries were run on a sequence (Hiseq, Illumina, Tokyo, Japan). The library preparation and sequencing were performed by Genewiz Strand-Specific RNA-seq service ...
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bioRxiv - Biophysics 2020Quote: The sequence of the nominal Illumina compatible amplicon was (with Illumina adapters and flow cell binding sequences in gray):
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bioRxiv - Cell Biology 2022Quote: ... The variable sequence was PCR-amplified and sequenced (Illumina HiSeq 4000) to verify clone representation of all library component ...
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bioRxiv - Evolutionary Biology 2022Quote: ... and data trimming (i.e., removal of the Illumina Universal Adapter sequences) was performed using Trimmomatic v0.39 tool (Bolger et al. ...
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bioRxiv - Microbiology 2022Quote: ... all plasmids expressing novel bNACHT genes were sequence verified by Illumina sequencing (CU Boulder Sequencing Facility) ...
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bioRxiv - Genomics 2022Quote: The demultiplexing of sequence data (from BCL files generated by Illumina sequencing systems to standard FASTQ file formats ...
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bioRxiv - Genomics 2022Quote: The demultiplexing of sequence data (from BCL files generated by Illumina sequencing systems to standard FASTQ file formats ...
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bioRxiv - Microbiology 2023Quote: ... FASTQ read sequence files were generated using bcl2fastq version 2.20 (Illumina). Initial quality assessment was based on data passing the Illumina Chastity filtering ...
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bioRxiv - Bioengineering 2023Quote: The genome sequences of representative edited clones were sequenced by Illumina technique ...
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bioRxiv - Microbiology 2023Quote: All datasets in this study consist of whole genome sequences (Illumina) of Mtb strains collected in countries with a generalized HIV epidemic.
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bioRxiv - Genomics 2023Quote: All animals imputed to sequence were initially genotyped on either (Illumina) Geneseek custom 50K or 25K SNP chips ...
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bioRxiv - Biophysics 2023Quote: ... Sequences were extracted in FastQ format using the bcl2fastq v2.19.1.403 (Illumina). After filtering for ribosomal contamination ...
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Spatial visualization of A-to-I Editing in cells using Endonuclease V Immunostaining Assay (EndoVIA)bioRxiv - Molecular Biology 2024Quote: ... Libraries were sequence using a NovaSeq X Plus 300 cycles (Illumina) to produce paired end 150-bp reads (approximately 30M reads per sample) ...
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bioRxiv - Cancer Biology 2019Quote: ... B with the TruSeq RNA Access Library Prep Kit (Illumina). RNA sequencing was performed in HiSeq 2500 (Illumina) ...
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bioRxiv - Microbiology 2023Quote: ... and TruSeq DNA Single Indexes Set A or B (Illumina), excluding the DNA fragmentation and clean-up of fragmented DNA steps ...
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bioRxiv - Microbiology 2019Quote: ... The Sequence library was prepared using a NexteraXT kit (Illumina, Cambridge, UK). Quality control and quantification of the cDNA and Sequence Library was performed using Quantifluor dsDNA System (Promega ...
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bioRxiv - Developmental Biology 2021Quote: ... Sequence information was extracted in FastQ format using the bcl2fastq v2.19.1.403 (Illumina).
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bioRxiv - Cell Biology 2019Quote: Sequence data was de-multiplexed using bcl2fastq2 Conversion Software v2.18 (Illumina Inc.) and quality analysed using FastQC ...
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bioRxiv - Physiology 2020Quote: ... Sequence data was de-multiplexed using bcl2fastq2 Conversion Software v2.18 (Illumina Inc.) and quality analysed using FastQC (http://www.bioinformatics.babraham.ac.uk/projects/fastqc) ...
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Differences in orthodenticle expression promote ommatidial size variation between Drosophila speciesbioRxiv - Evolutionary Biology 2021Quote: ... Sequence images were transformed to bcl files using the software BaseCaller (Illumina). The bcl files were demultiplexed to fastq files with CASAVA (version 1.8.2).
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bioRxiv - Microbiology 2021Quote: Sequence reads were demultiplexed using MiSeq Reporter software version 2.5.0.5 (Illumina Inc) and analyzed using Quantitative Insights Into Microbial Ecology 2 (QIIME2 ...
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bioRxiv - Biochemistry 2022Quote: ... The sequences of the DNAs were analyzed using the NovaSeq6000 platform (Illumina) at Macrogen (Japan) ...
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bioRxiv - Genomics 2022Quote: We did not analyze raw RNA-seq data (i.e., Illumina sequence reads) for two of the infection datasets ...
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bioRxiv - Genetics 2022Quote: ... and the paired obtained sequences (terminal 125 bp) were analyzed by Illumina Hi-Seq 2500 system (Illumina ...
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bioRxiv - Microbiology 2020Quote: ... The Sequence library was prepared using a NexteraXT kit (Illumina, Cambridge, UK). Quality control and quantification of the cDNA and Sequence Library was performed using Quantifluor dsDNA System (Promega ...
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bioRxiv - Genomics 2020Quote: ... RNAseq libraries were paired-end sequences on a NovaSeq 6000 system (Illumina). Minimum 80 million reads were obtained per sample ...
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bioRxiv - Molecular Biology 2020Quote: ... 50-bp single-end sequences were obtained using the HiSeq4000 sequencer (Illumina) in Vincent J ...
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bioRxiv - Microbiology 2021Quote: Nextera XT adapters were removed and sequence reads were trimmed from Illumina paired-end reads (2×150 bp ...
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bioRxiv - Genomics 2020Quote: We screened a large collection of publicly available whole genome sequences (Illumina) of MTBC strains belonging to L1 and L3 ...