Evidence map›Paper›PMID 31189906›Full record

ReviewHeredity2019

Patterns in the genome.

Wendy A Bickmore

Open access · bronzeAbstract readReview
In one paragraph

Review in Heredity, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Wendy A BickmoreMRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine at the University of Edinburgh, Crewe Road, Edinburgh, EH42XU, UK. Wendy.Bickmore@igmm.ed.ac.uk.ORCID http://orcid.org/0000-0001-6660-7735
Institute of Genetics and Cancer · GB

Funding

Medical Research Council MC_UU_00007/2RCUK | Medical Research Council (MRC) MC_ UU_00007/2
6 · The paper itself

Abstract

The human genome is not randomly organised, with respect to both the linear organisation of the DNA sequence along chromosomes and to the spatial organisation of chromosomes in the cell nucleus. Here I discuss how these patterns of sequence organisation were first discovered by molecular biologists and how they relate to the patterns revealed decades earlier by cytogeneticists and manifest as chromosome bands.

Indexed as

Chromosome MappingChromosomes, HumanGenome, HumanChromosome BandingCpG IslandsDNA MethylationGenomicsHumansIn Situ Hybridization, FluorescenceOligonucleotide Array Sequence Analysis

Identifiers

PMID31189906
PMCPMC6781130
OpenAlexW2950566814

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.