(Q57046462)

5

0 references

Fritz Sedlazeck

object named as

Fritz J Sedlazeck

1

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Michael C. Schatz

object named as

Michael C Schatz

7

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author name string

Philipp Rescheneder

2

0 references

Han Fang

4

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Arndt von Haeseler

https://scigraph.springernature.com/pub.10.1038/s41592-018-0001-7

6

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language of work or name

English

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publication date

June 2018

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published in

Nature Methods

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volume

15

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issue

6

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page(s)

461-468

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exact match

0 references

cites work

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2 November 2018

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Long-read genome sequencing identifies causal structural variation in a Mendelian disease.

2 November 2018

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Copy number increases of transposable elements and protein-coding genes in an invasive fish of hybrid origin

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Genomic Rearrangements in Arabidopsis Considered as Quantitative Traits

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2 November 2018

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Resolving the complexity of the human genome using single-molecule sequencing

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Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls

2 November 2018

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2 November 2018

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On the power and the systematic biases of the detection of chromosomal inversions by paired-end genome sequencing.

2 November 2018

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Phenotypic impact of genomic structural variation: insights from and for human disease

2 November 2018

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2 November 2018

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Low-copy repeats at the human VIPR2 gene predispose to recurrent and nonrecurrent rearrangements.

2 November 2018

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2 November 2018

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2 November 2018

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2 November 2018

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Pelizaeus-Merzbacher disease caused by a duplication-inverted triplication-duplication in chromosomal segments including the PLP1 region.

2 November 2018

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Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci

2 November 2018

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Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome

2 November 2018

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2 November 2018

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2 November 2018

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2 November 2018

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Adaptive seeds tame genomic sequence comparison

2 November 2018

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The Sequence Alignment/Map format and SAMtools

2 November 2018

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2 November 2018

Assembly reconciliation

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Recurrent inversion with concomitant deletion and insertion events in the coagulation factor VIII gene suggests a new mechanism for X-chromosomal rearrangements causing hemophilia A.

2 November 2018

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APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

2 November 2018

1 reference

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Large-scale copy number polymorphism in the human genome

2 November 2018

1 reference

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Algorithms on Strings, Trees, and Sequences

2 November 2018

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Crossref

https://api.crossref.org/works/10.1038%2FS41592-018-0001-7