… We suggest that dbSNP be referenced as follows: Sherry,ST, Ward,M. and Sirotkin,K. (1999)
dbSNP—Database for Single Nucleotide Polymorphisms and Other Classes of Minor …

The variant call format (VCF) is a generic format for storing DNA polymorphism data such as
SNPs, insertions, deletions and structural variants, together with rich annotations. VCF is …

… It has been estimated that, in the world’s human population, about 10 million sites (that is,
one variant per 300 bases on average) vary such that both alleles are observed at a frequency …

… Tracks may be visualized in either the NCBI or UCSC genome viewers or may be downloaded
to the user’s computer for local analysis. Data from the Roadmap Epigenomics project, …

In addition to maintaining the GenBank(R) nucleic acid sequence database, the National
Center for Biotechnology Information (NCBI) provides analysis and retrieval resources for the …

We present the first results of the Fermilab National Accelerator Laboratory (FNAL) Muon g−
2 Experiment for the positive muon magnetic anomaly a μ≡(g μ− 2)/2. The anomaly is …

Stereotactic thalamotomy of the thalamic nucleus ventralis intermedius (VIM) is routinely used
for movement disorders. During this procedure, it has been observed that high-frequency (…

Purpose We sought to describe and validate an automated image registration method (AIR
3.0) based on matching of voxel intensities. Method Different cost functions, different …

Exploiting rich administrative data and salient policy variation, we study the substitution
between illegal tax evasion and legal tax avoidance. By increasing its enforcement effort, the …

… Final images were generated from data collected for 70 s following the arrival of the tracer
in the brain. Attenuation correction was performed using 20 min transmission scans acquired …