NCBI . NLM . NIH . GOV {
}
We began analyzing https://pmc.ncbi.nlm.nih.gov/articles/PMC7768885/, but it redirected us to https://pmc.ncbi.nlm.nih.gov/articles/PMC7768885/. The analysis below is for the second page.
Title[redir]:
Nanopore native RNA sequencing of a human poly(A) transcriptome - PMC
Description:
High throughput cDNA sequencing technologies have advanced our understanding of transcriptome complexity and regulation. However, these methods lose information contained in biological RNA because the copied reads are often short and because ...
Title[redir]:
Nanopore native RNA sequencing of a human poly(A) transcriptome - PMC
Description:
High throughput cDNA sequencing technologies have advanced our understanding of transcriptome complexity and regulation. However, these methods lose information contained in biological RNA because the copied reads are often short and because ...
Matching Content Categories {📚}
- Education
- Science
- Telecommunications
Content Management System {📝}
What CMS is ncbi.nlm.nih.gov built with?
Custom-built
No common CMS systems were detected on Ncbi.nlm.nih.gov, and no known web development framework was identified.
Traffic Estimate {📈}
What is the average monthly size of ncbi.nlm.nih.gov audience?
🌠 Phenomenal Traffic: 5M - 10M visitors per month
Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Ncbi.nlm.nih.gov Make Money? {💸}
We don't see any clear sign of profit-making.
Many websites are intended to earn money, but some serve to share ideas or build connections. Websites exist for all kinds of purposes. This might be one of them. Ncbi.nlm.nih.gov might be earning cash quietly, but we haven't detected the monetization method.
Keywords {🔍}
rna, reads, polya, sequencing, doi, nanopore, pubmed, google, scholar, length, read, isoforms, figure, pmc, article, data, genes, free, current, analysis, supplementary, ont, isoform, native, cdna, methods, cell, ionic, human, tail, strand, sequence, set, transcript, gencode, genome, modifications, mrna, transcripts, gene, nat, version, aligned, signal, transcriptome, base, supptable, dna, splicing, transcription,
Topics {✒️}
/nanopore-wgs-consortium/na12878/tree/master/nanopore-human-transcriptome/scripts/bulk_signal_read_correction /nanopore-wgs-consortium/na12878/tree/master/nanopore-human-transcriptome/scripts] /nanopore-wgs-consortium/na12878/tree/master/nanopore-human-transcriptome/scripts /nanopore-wgs-consortium/na12878/blob/master/rna /nanopore-wgs-consortium/na12878 gov/1000genomes/ftp/technical/reference/grch38_reference_genome/ /1000genomes/ftp/technical/reference/grch38_reference_genome nanopore-human-transcriptome/scripts single-molecule long-read transcriptome suppnote1andsupptables nihms1540455-supplement-suppnote1andsupptables 1540455_supptable2 nihms1540455-supplement-1540455_supptable2 1540455_supptable5 nihms1540455-supplement-1540455_supptable5 1540455_supptable6 nihms1540455-supplement-1540455_supptable6 1540455_supptable7 nihms1540455-supplement-1540455_supptable7 1540455_supptable11 nihms1540455-supplement-1540455_supptable11 1540455_supptable12 nihms1540455-supplement-1540455_supptable12 1540455_supptable14 nihms1540455-supplement-1540455_supptable14 1540455_supptable3 nihms1540455-supplement-1540455_supptable3 encode chip-seq data18 intron-free transcripts identified encode chip-seq data pmc beta search n6-methyladenosine–encoded epitranscriptomics high-throughput nanopore sequencing high-resolution transcriptome analysis primer-directed enzymatic amplification examine allele-specific expression rna-dependent dna polymerase m6a-laic-seq reveals illumina short-read sequencing strong linear anti-correlation health research consortium full-length transcriptome identification modulating rna-protein binding mt-nd4l/nd4 transcripts short-read sbs data27 mitochondrial protein-coding transcripts mt-nd4l/nd4 genes nucleotides providing splice-variant nuclease free water data availability statements long-read rna sequencing gencode-based isoform sets spring-loaded base modification haplotype-sensitive assembler hapcut223 higher accuracy short-reads conventional short-read sequencing full-length fraction declined flair-sensitive data-set including mrna stability
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External Links {🔗}(129)
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